US20020019554A1 - Dithiocarboxylic ester synthetic process - Google Patents
Dithiocarboxylic ester synthetic process Download PDFInfo
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- US20020019554A1 US20020019554A1 US09/877,455 US87745501A US2002019554A1 US 20020019554 A1 US20020019554 A1 US 20020019554A1 US 87745501 A US87745501 A US 87745501A US 2002019554 A1 US2002019554 A1 US 2002019554A1
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- 0 *SC(*)=S Chemical compound *SC(*)=S 0.000 description 4
- XFOILLZVZVQIPH-UHFFFAOYSA-N C=C(C)C.II Chemical compound C=C(C)C.II XFOILLZVZVQIPH-UHFFFAOYSA-N 0.000 description 4
- GDQOERDCQIDSAE-UHFFFAOYSA-M CC(=S)SC(C)(C)C.CCC(C)SC(C)=S.[V]I Chemical compound CC(=S)SC(C)(C)C.CCC(C)SC(C)=S.[V]I GDQOERDCQIDSAE-UHFFFAOYSA-M 0.000 description 4
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- NULMRDSYVCBQAQ-UHFFFAOYSA-N CC(C)(SC(=O)C1=CC=CC=C1)C1=CC=CC=C1.CC(CC1=CC=CC=C1)SC(=O)C1=CC=CC=C1 Chemical compound CC(C)(SC(=O)C1=CC=CC=C1)C1=CC=CC=C1.CC(CC1=CC=CC=C1)SC(=O)C1=CC=CC=C1 NULMRDSYVCBQAQ-UHFFFAOYSA-N 0.000 description 1
- KOBJYYDWSKDEGY-UHFFFAOYSA-N CC(C)(SC(=S)C1=CC=CC=C1)C1=CC=CC=C1 Chemical compound CC(C)(SC(=S)C1=CC=CC=C1)C1=CC=CC=C1 KOBJYYDWSKDEGY-UHFFFAOYSA-N 0.000 description 1
- GBGTVZFBNVQHOI-UHFFFAOYSA-N CC(CC1=CC=CC=C1)SC(=S)C1=CC=CC=C1 Chemical compound CC(CC1=CC=CC=C1)SC(=S)C1=CC=CC=C1 GBGTVZFBNVQHOI-UHFFFAOYSA-N 0.000 description 1
- JWQFTRPGGKABPC-UHFFFAOYSA-N CC(SC(=O)C1=CC=CC=C1)C1=CC=CC=C1.O=C(SCCC1=CC=CC=C1)C1=CC=CC=C1 Chemical compound CC(SC(=O)C1=CC=CC=C1)C1=CC=CC=C1.O=C(SCCC1=CC=CC=C1)C1=CC=CC=C1 JWQFTRPGGKABPC-UHFFFAOYSA-N 0.000 description 1
- LPQAZPBLCKNKOE-UHFFFAOYSA-N CC1=CC=C(C(C)SC(=O)C2=CC=CC=C2)C=C1.CC1=CC=C(CCSC(=O)C2=CC=CC=C2)C=C1 Chemical compound CC1=CC=C(C(C)SC(=O)C2=CC=CC=C2)C=C1.CC1=CC=C(CCSC(=O)C2=CC=CC=C2)C=C1 LPQAZPBLCKNKOE-UHFFFAOYSA-N 0.000 description 1
- QUVRZTNDORKYOH-UHFFFAOYSA-N CC1=CC=C(C(C)SC(=S)C2=CC=CC=C2)C=C1 Chemical compound CC1=CC=C(C(C)SC(=S)C2=CC=CC=C2)C=C1 QUVRZTNDORKYOH-UHFFFAOYSA-N 0.000 description 1
- QOIRRBXKVLIHSE-UHFFFAOYSA-N CC1=CC=C(CCSC(=S)C2=CC=CC=C2)C=C1 Chemical compound CC1=CC=C(CCSC(=S)C2=CC=CC=C2)C=C1 QOIRRBXKVLIHSE-UHFFFAOYSA-N 0.000 description 1
- BXGRZOBZOCICFS-UHFFFAOYSA-N CCC(C)(C(NN)=N)N Chemical compound CCC(C)(C(NN)=N)N BXGRZOBZOCICFS-UHFFFAOYSA-N 0.000 description 1
- ZCFPBINVCWBGOK-UHFFFAOYSA-N CCCCC(C)SC(=O)C1=CC=CC=C1.CCCCCCSC(=O)C1=CC=CC=C1 Chemical compound CCCCC(C)SC(=O)C1=CC=CC=C1.CCCCCCSC(=O)C1=CC=CC=C1 ZCFPBINVCWBGOK-UHFFFAOYSA-N 0.000 description 1
- KKKQQFOJGQSEHN-UHFFFAOYSA-N CCCCC(C)SC(=S)C1=CC=CC=C1 Chemical compound CCCCC(C)SC(=S)C1=CC=CC=C1 KKKQQFOJGQSEHN-UHFFFAOYSA-N 0.000 description 1
- ZNHDAXOYXZVUSV-UHFFFAOYSA-N CCCCCCSC(=S)C1=CC=CC=C1 Chemical compound CCCCCCSC(=S)C1=CC=CC=C1 ZNHDAXOYXZVUSV-UHFFFAOYSA-N 0.000 description 1
- HKOHABYBCFQSGP-UHFFFAOYSA-N COC(=O)C(C)(C)SC(=O)C1=CC=CC=C1.COC(=O)C(C)CSC(=O)C1=CC=CC=C1 Chemical compound COC(=O)C(C)(C)SC(=O)C1=CC=CC=C1.COC(=O)C(C)CSC(=O)C1=CC=CC=C1 HKOHABYBCFQSGP-UHFFFAOYSA-N 0.000 description 1
- OCZWUHHTESEIHR-UHFFFAOYSA-N COC(=O)C(C)(C)SC(=S)C1=CC=CC=C1 Chemical compound COC(=O)C(C)(C)SC(=S)C1=CC=CC=C1 OCZWUHHTESEIHR-UHFFFAOYSA-N 0.000 description 1
- SVJXGTHONYSMHV-UHFFFAOYSA-N COC(=O)C(C)CSC(=S)C1=CC=CC=C1 Chemical compound COC(=O)C(C)CSC(=S)C1=CC=CC=C1 SVJXGTHONYSMHV-UHFFFAOYSA-N 0.000 description 1
- JXPLECNKPVHWMG-UHFFFAOYSA-N S=C(SCCC1=CC=CC=C1)C1=CC=CC=C1 Chemical compound S=C(SCCC1=CC=CC=C1)C1=CC=CC=C1 JXPLECNKPVHWMG-UHFFFAOYSA-N 0.000 description 1
- GQOKQOBQBFMLSK-UHFFFAOYSA-N S=P1([Ar])SP(=S)([Ar])S1 Chemical compound S=P1([Ar])SP(=S)([Ar])S1 GQOKQOBQBFMLSK-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C327/00—Thiocarboxylic acids
- C07C327/36—Esters of dithiocarboxylic acids
Definitions
- the invention relates to dithiocarboxylic esters and processes for the preparation thereof.
- Living polymerization is a method by which polymers having a narrow molecular weight distribution may be obtained.
- Block copolymers may also be synthesized using the method.
- Block copolymers may display improved mechanical and/or chemical properties over corresponding random copolymers.
- Commercial processes for the production of block copolymers typically employ anionic initiators in living polymerization processes. Polymerization processes using free radical initiators have many attractive characteristics and have attained commercial importance. However, these do not include processes with characteristics of living polymerization.
- RAFT addition-fragmentation chain transfer
- chain transfer agents for RAFT polymerizations is described in International Application Number PCT/US97/12540, published as WO 98/01478 on Jan. 15 1998. Free radical processes employing these chain transfer agents resulted in polymers having low polydispersity in bulk, emulsion and solution polymerizations. Block copolymers were also successfully prepared.
- Disadvantages of these methods include safety, cost and sensitivity concerns regarding the use of Grignard reagents, inability to utilize desirable probe functionalities because of incompatibility with reagents, lack of suitable thiol, thioacid and/or disulfide precursors and, ultimately, low yield from the reactions. It is therefore an object of the present invention to provide a process for the synthesis of dithiocarboxylic esters that eliminates the use of Grignard reagents, allows for synthesis of functional dithiocarboxylic esters, requires inexpensive and readily available starting materials, and provides high yields.
- [0008] comprises reacting a carboxylic acid compound of formula R 1 (COOH) m , a compound of formula R 2 AH and phosphorus pentasulfide, wherein R 1 is a m-valent radical selected from the group consisting of alkyl, substituted alkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl; R 2 is selected from the group consisting of alkyl, substituted alkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, alkylaryl, and substituted alkylaryl; A is S or O; and m is an integer from 1-6.
- a process according to the present invention comprises:
- R 3 is selected from the group consisting of alkyl, substituted alkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl;
- R 4 is a n-valent radical selected from the group consisting of alkyl, substituted alkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl;
- R 5 is H or lower alkyl; and
- A is S or O.
- alkyl is intended to include linear, branched, or cyclic hydrocarbon structures and combinations thereof.
- Lower alkyl refers to alkyl groups of from 1 to 4 carbon atoms. Examples of lower alkyl groups include methyl, ethyl, propyl, isopropyl, butyl, s-and t-butyl. Preferred alkyl groups are those of C 20 or below.
- Cycloalkyl is a subset of alkyl and includes cyclic hydrocarbon groups of from 3 to 8 carbon atoms. Examples of cycloalkyl groups include c-propyl, c-butyl, c-pentyl, and norbornyl
- Alkoxy or alkoxyl refers to groups of from 1 to 8 carbon atoms of a straight, branched, cyclic configuration and combinations thereof attached to the parent structure through an oxygen. Examples include methoxy, ethoxy, propoxy, isopropoxy, cyclopropyloxy, and cyclohexyloxy. Lower alkoxy refers to groups containing one to four carbons.
- Acyl refers to groups of from 1 to 8 carbon atoms of a straight, branched, cyclic configuration, saturated, unsaturated and aromatic and combinations thereof, attached to the parent structure through a carbonyl functionality.
- One or more carbons in the acyl residue may be replaced by nitrogen, oxygen or sulfur as long as the point of attachment to the parent remains at the carbonyl. Examples include acetyl, benzoyl, propionyl, isobutyryl, t-butoxycarbonyl, and benzyloxycarbonyl.
- Lower-acyl refers to groups containing one to four carbons.
- Aryl and heteroaryl mean a 5- or 6-membered aromatic or heteroaromatic ring containing 0-3 heteroatoms selected from nitrogen, oxygen or sulfur; a bicyclic 9- or 10-membered aromatic or heteroaromatic ring system containing 0-3 heteroatoms selected from Nitrogen, oxygen or sulfur; or a tricyclic 13- or 14-membered aromatic or heteroaromatic ring system containing 0-3 heteroatoms selected from Nitrogen, oxygen or sulfur.
- Each of these rings is optionally substituted with 1-3 lower alkyl, substituted alkyl, substituted alkynyl, carbonyl, nitro, halogen, haloalkyl, hydroxy, alkoxy, OCH(COOH) 2 , cyano, primary amino, secondary amino, acylamino, phenyl, benzyl, phenoxy, benzyloxy, heteroaryl, or heteroaryloxy; each of said phenyl, benzyl, phenoxy, benzyloxy, heteroaryl, and heteroaryloxy is optionally substituted with 1-3 substitutents selected from lower alkyl, alkenyl, alkynyl, halogen, hydroxy, haloalkyl, alkoxy, cyano, phenyl, benzyl, benzyloxy, carboxamido, heteroaryl, heteroaryloxy, nitro or —NRR (wherein R is independently H, lower alkyl or cycloalkyl, and
- the aromatic 6- to 14-membered carbocyclic rings include, for example, benzene, naphthalene, indane, tetralin, and fluorene; and the 5- to 10-membered aromatic heterocyclic rings include, e.g., imidazole, pyridine, indole, thiophene, benzopyranone, thiazole, furan, benzimidazole, quinoline, isoquinoline, quinoxaline, pyrimidine, pyrazine, tetrazole and pyrazole.
- Alkylaryl means an alkyl residue attached to an aryl ring. Examples are benzyl and phenethyl. Heteroarylalkyl means an alkyl residue attached to a heteroaryl ring. Examples include pyridinylmethyl and pyrimidinylethyl.
- Heterocycle means a cycloalkyl or aryl residue in which one to two of the carbons is replaced by a heteroatom such as oxygen, nitrogen or sulfur.
- heterocycles that fall within the scope of the invention include pyrrolidine, pyrazole, pyrrole, indole, quinoline, isoquinoline, tetrahydroisoquinoline, benzofuran, benzodioxan, benzodioxole (commonly referred to as methylenedioxyphenyl, when occurring as a substituent), tetrazole, morpholine, thiazole, pyridine, pyridazine, pyrimidine, thiophene, furan, oxazole, oxazoline, isoxazole, dioxane, and tetrahydrofuran.
- Substituted alkyl, aryl, cycloalkyl, or heterocyclyl refer to alkyl, aryl, cycloalkyl, or heterocyclyl wherein up to three H atoms in each residue are replaced with halogen, haloalkyl, hydroxy, lower alkoxy, carboxy, carboalkoxy, carboxamido, cyano, carbonyl, nitro, primary amino, secondary amino, alkylthio, sulfoxide, sulfone, acylamino, amidino, phenyl, benzyl, heteroaryl, phenoxy, benzyloxy, heteroaryloxy, or substituted phenyl, benzyl, heteroaryl, phenoxy, benzyloxy, or heteroaryloxy.
- the present invention relates to dithiocarboxylic esters having the following structures:
- a process according to the present invention comprises reacting a carboxylic acid compound of formula R 1 (COOH) m , a compound of formula R 2 AH and phosphorus pentasulfide, to form a dithiocarboxylic ester of structure I,
- R 1 represents a m-valent radical selected from the group consisting of alkyl, substituted alkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl
- R 2 represents alkyl, substituted alkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, alkylaryl, and substituted alkylaryl
- A represents S or O
- m is an integer from 1-6.
- Preferred dithiocarboxylic esters that may be prepared by the process are benzyl dithiobenzoate, benzyl-4-methoxydithiobenzoate, benzyl-4-fluorodithiobenzoate, benzyl-4-nitrodithiobenzoate, benzyl-4-cyanodithiobenzoate, benzyl-4-trifluoromethyldithiobenzoate, diphenyidithiobenzoate, propyl dithiobenzoate, benzyl dithiopropionate, and benzyl-4-chlorodithiobenzoate.
- Phosphorus pentasulfide is known as a thiating agent for amides, ketones, aldehydes, esters, and thioesters. Typically, a 1:1:1 proportion of acid to alcohol/thiol to phosphorus pentasulfide is used. In some cases, it may be necessary to use an excess of the reagent to convert the esters to dithioesters. It will be noted that where substitutents of the substituted alkyl, aryl, alkylaryl or heteroaryl groups are amides, ketones, aldehydes, or esters, these groups may or may not be converted by the thiating agent to the corresponding S-containing compound. If an undesired conversion is expected to occur, it may be avoided by protecting the groups with a suitable protecting agent.
- a process according to the present invention comprises reacting a compound of formula R 3 (COAH) m and a compound having structure II
- R 3 may be alkyl, substituted alkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl;
- R 4 is a n-valent radical selected from the group consisting of alkyl, substituted alkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl;
- R 5 is H or lower alkyl;
- A is S or O; and
- Preferred dithiocarboxylic esters 1-10 that may be prepared by the process are shown in Table 1. TABLE 1
- Thiating agents include phosphorus pentasulfide or Lawesson's reagent, 2,4-bis-(4-methoxyphenyl)-1,3,2,4-dithiadiphosphetane 2,4-disulfide.
- the thiating agent is Lawesson's reagent.
- substituent groups including amides, ketones, aldehydes, or esters, may or may not be converted by the thiating agent to the corresponding S-containing compound.
- substituent groups including amides, ketones, aldehydes, or esters
- thiobenzoic acid and methylmethacrylate (MMA) according to Scheme B, the thioester group was converted to a dithioester, while the ester derived from MMA remained unconverted.
- the convertible group may be masked with a protecting group.
- Suitable compounds of structure II include vinyl compounds, olefins, acrylates and methacrylates and styrene and styrene derivatives.
- Preferred compounds of this type are vinyl acetate, acrylate and methacrylate esters, styrene, ⁇ -methylstyrene and p-methylstyrene.
- Divalent compounds, such as divinylbenzene, may also be used.
- Suitable solvents for the reactions of Schemes A and B typically include ethers, aromatics, tertiary amines and chlorinated solvents pyridine, DMF, dioxane, acetonitrile, and THF. Toluene and benzene are preferred solvents. As phosphorus pentasulfide reacts with DMSO, primary and secondary amines, alcohols and neutral or acidic water, these solvents are generally avoided.
- a 50-ml round bottomed flask under nitrogen atmosphere was charged with 20 g of benzene, 100 mg of Montmorillonite (K-10) clay as catalyst, 0.86 g of ⁇ -methylstyrene and 1 g of thiobenzoic acid.
- the mixture was degassed with nitrogen for 15 minutes.
- the heterogeneous mixture was heated to reflux over the course of 10 minutes.
- the thiobenzoic acid conversion was determined by GC-MS.
- the unreacted thiobenzoic acid was washed off completely using aqueous base (NaHCO3).
- the resulting product was analyzed by GC-MS, 1 H and 13C NMR.
- the conversion of thiobenzoic acid after 960 minutes was 80% and the selectivity for the product 5 and 6 was 76% and 3% respectively.
Abstract
Description
- The invention relates to dithiocarboxylic esters and processes for the preparation thereof.
- Living polymerization is a method by which polymers having a narrow molecular weight distribution may be obtained. Block copolymers may also be synthesized using the method. Block copolymers may display improved mechanical and/or chemical properties over corresponding random copolymers. Commercial processes for the production of block copolymers typically employ anionic initiators in living polymerization processes. Polymerization processes using free radical initiators have many attractive characteristics and have attained commercial importance. However, these do not include processes with characteristics of living polymerization.
-
- as chain transfer agents for RAFT polymerizations is described in International Application Number PCT/US97/12540, published as WO 98/01478 on Jan. 15 1998. Free radical processes employing these chain transfer agents resulted in polymers having low polydispersity in bulk, emulsion and solution polymerizations. Block copolymers were also successfully prepared.
- However, known methods for synthesis of the chain transfer agents are unsatisfactory for various reasons. Literature methods for preparation of dithiocarboxylic esters include: alkylation of ArCS2M (M=Na or K) or ArCS2MgX with an appropriate alkyl or aryl halide, thiation of S-substituted thioesters using Lawesson's reagent, transesterifications of dithioesters with thiols, and reaction of bis(thiocarbonyl)disulfides with azo compounds. Disadvantages of these methods include safety, cost and sensitivity concerns regarding the use of Grignard reagents, inability to utilize desirable probe functionalities because of incompatibility with reagents, lack of suitable thiol, thioacid and/or disulfide precursors and, ultimately, low yield from the reactions. It is therefore an object of the present invention to provide a process for the synthesis of dithiocarboxylic esters that eliminates the use of Grignard reagents, allows for synthesis of functional dithiocarboxylic esters, requires inexpensive and readily available starting materials, and provides high yields.
- It has been unexpectedly discovered that the processes of the present invention provide an improved method for the synthesis of dithiocarboxylic esters which meets these requirements. In addition, the process operates under mild conditions, and provides for facile isolation of products.
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- comprises reacting a carboxylic acid compound of formula R1(COOH)m, a compound of formula R2AH and phosphorus pentasulfide, wherein R1 is a m-valent radical selected from the group consisting of alkyl, substituted alkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl; R2 is selected from the group consisting of alkyl, substituted alkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, alkylaryl, and substituted alkylaryl; A is S or O; and m is an integer from 1-6.
- In another aspect, a process according to the present invention comprises:
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- in the presence of a clay catalyst; and
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- wherein R3 is selected from the group consisting of alkyl, substituted alkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl; R4 is a n-valent radical selected from the group consisting of alkyl, substituted alkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl; R5 is H or lower alkyl; and A is S or O.
- In the context of the present invention, alkyl is intended to include linear, branched, or cyclic hydrocarbon structures and combinations thereof. Lower alkyl refers to alkyl groups of from 1 to 4 carbon atoms. Examples of lower alkyl groups include methyl, ethyl, propyl, isopropyl, butyl, s-and t-butyl. Preferred alkyl groups are those of C20 or below. Cycloalkyl is a subset of alkyl and includes cyclic hydrocarbon groups of from 3 to 8 carbon atoms. Examples of cycloalkyl groups include c-propyl, c-butyl, c-pentyl, and norbornyl
- Alkoxy or alkoxyl refers to groups of from 1 to 8 carbon atoms of a straight, branched, cyclic configuration and combinations thereof attached to the parent structure through an oxygen. Examples include methoxy, ethoxy, propoxy, isopropoxy, cyclopropyloxy, and cyclohexyloxy. Lower alkoxy refers to groups containing one to four carbons.
- Acyl refers to groups of from 1 to 8 carbon atoms of a straight, branched, cyclic configuration, saturated, unsaturated and aromatic and combinations thereof, attached to the parent structure through a carbonyl functionality. One or more carbons in the acyl residue may be replaced by nitrogen, oxygen or sulfur as long as the point of attachment to the parent remains at the carbonyl. Examples include acetyl, benzoyl, propionyl, isobutyryl, t-butoxycarbonyl, and benzyloxycarbonyl. Lower-acyl refers to groups containing one to four carbons.
- Aryl and heteroaryl mean a 5- or 6-membered aromatic or heteroaromatic ring containing 0-3 heteroatoms selected from nitrogen, oxygen or sulfur; a bicyclic 9- or 10-membered aromatic or heteroaromatic ring system containing 0-3 heteroatoms selected from Nitrogen, oxygen or sulfur; or a tricyclic 13- or 14-membered aromatic or heteroaromatic ring system containing 0-3 heteroatoms selected from Nitrogen, oxygen or sulfur. Each of these rings is optionally substituted with 1-3 lower alkyl, substituted alkyl, substituted alkynyl, carbonyl, nitro, halogen, haloalkyl, hydroxy, alkoxy, OCH(COOH)2, cyano, primary amino, secondary amino, acylamino, phenyl, benzyl, phenoxy, benzyloxy, heteroaryl, or heteroaryloxy; each of said phenyl, benzyl, phenoxy, benzyloxy, heteroaryl, and heteroaryloxy is optionally substituted with 1-3 substitutents selected from lower alkyl, alkenyl, alkynyl, halogen, hydroxy, haloalkyl, alkoxy, cyano, phenyl, benzyl, benzyloxy, carboxamido, heteroaryl, heteroaryloxy, nitro or —NRR (wherein R is independently H, lower alkyl or cycloalkyl, and —RR may be fused to form a cyclic ring with nitrogen). The aromatic 6- to 14-membered carbocyclic rings include, for example, benzene, naphthalene, indane, tetralin, and fluorene; and the 5- to 10-membered aromatic heterocyclic rings include, e.g., imidazole, pyridine, indole, thiophene, benzopyranone, thiazole, furan, benzimidazole, quinoline, isoquinoline, quinoxaline, pyrimidine, pyrazine, tetrazole and pyrazole.
- Alkylaryl means an alkyl residue attached to an aryl ring. Examples are benzyl and phenethyl. Heteroarylalkyl means an alkyl residue attached to a heteroaryl ring. Examples include pyridinylmethyl and pyrimidinylethyl.
- Heterocycle means a cycloalkyl or aryl residue in which one to two of the carbons is replaced by a heteroatom such as oxygen, nitrogen or sulfur. Examples of heterocycles that fall within the scope of the invention include pyrrolidine, pyrazole, pyrrole, indole, quinoline, isoquinoline, tetrahydroisoquinoline, benzofuran, benzodioxan, benzodioxole (commonly referred to as methylenedioxyphenyl, when occurring as a substituent), tetrazole, morpholine, thiazole, pyridine, pyridazine, pyrimidine, thiophene, furan, oxazole, oxazoline, isoxazole, dioxane, and tetrahydrofuran.
- Substituted alkyl, aryl, cycloalkyl, or heterocyclyl refer to alkyl, aryl, cycloalkyl, or heterocyclyl wherein up to three H atoms in each residue are replaced with halogen, haloalkyl, hydroxy, lower alkoxy, carboxy, carboalkoxy, carboxamido, cyano, carbonyl, nitro, primary amino, secondary amino, alkylthio, sulfoxide, sulfone, acylamino, amidino, phenyl, benzyl, heteroaryl, phenoxy, benzyloxy, heteroaryloxy, or substituted phenyl, benzyl, heteroaryl, phenoxy, benzyloxy, or heteroaryloxy.
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-
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- where R1 represents a m-valent radical selected from the group consisting of alkyl, substituted alkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl; R2 represents alkyl, substituted alkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, alkylaryl, and substituted alkylaryl; A represents S or O; and m is an integer from 1-6. This process is illustrated in Scheme A. In the scheme, one equivalent of a carboxylic acid compound reacts with one equivalent of an alcohol or thiol in the presence of one equivalent of phosphorus pentasulfide. Preferred dithiocarboxylic esters that may be prepared by the process are benzyl dithiobenzoate, benzyl-4-methoxydithiobenzoate, benzyl-4-fluorodithiobenzoate, benzyl-4-nitrodithiobenzoate, benzyl-4-cyanodithiobenzoate, benzyl-4-trifluoromethyldithiobenzoate, diphenyidithiobenzoate, propyl dithiobenzoate, benzyl dithiopropionate, and benzyl-4-chlorodithiobenzoate.
- Phosphorus pentasulfide is known as a thiating agent for amides, ketones, aldehydes, esters, and thioesters. Typically, a 1:1:1 proportion of acid to alcohol/thiol to phosphorus pentasulfide is used. In some cases, it may be necessary to use an excess of the reagent to convert the esters to dithioesters. It will be noted that where substitutents of the substituted alkyl, aryl, alkylaryl or heteroaryl groups are amides, ketones, aldehydes, or esters, these groups may or may not be converted by the thiating agent to the corresponding S-containing compound. If an undesired conversion is expected to occur, it may be avoided by protecting the groups with a suitable protecting agent.
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- As noted above, substituent groups, including amides, ketones, aldehydes, or esters, may or may not be converted by the thiating agent to the corresponding S-containing compound. For example, in a reaction between thiobenzoic acid and methylmethacrylate (MMA) according to Scheme B, the thioester group was converted to a dithioester, while the ester derived from MMA remained unconverted. If desired, the convertible group may be masked with a protecting group.
- Suitable compounds of structure II include vinyl compounds, olefins, acrylates and methacrylates and styrene and styrene derivatives. Preferred compounds of this type are vinyl acetate, acrylate and methacrylate esters, styrene, α-methylstyrene and p-methylstyrene. Divalent compounds, such as divinylbenzene, may also be used.
- Suitable solvents for the reactions of Schemes A and B typically include ethers, aromatics, tertiary amines and chlorinated solvents pyridine, DMF, dioxane, acetonitrile, and THF. Toluene and benzene are preferred solvents. As phosphorus pentasulfide reacts with DMSO, primary and secondary amines, alcohols and neutral or acidic water, these solvents are generally avoided.
- The reactions in Scheme A and B proceed under a wide range of temperature conditions, and preferably, from about 0° C. to about 150° C. More preferably, the temperature ranges from about 80° C. to about 110° C.
- In order to fully illustrate the nature of the present invention and the manner of practicing the same, the following examples are presented:
- A mixture of benzoic acid (1.22 g), benzyl mercaptan (1.24 g) and phosphorus pentasulfide (4.44 g) in toluene (40 ml) was refluxed for 10 h. A dark red color was developed immediately after heating. After the reaction was complete (as monitored by GC-MS), it was cooled to room temperature and purified by column chromatography packed with neutral alumina, eluting with benzene. Removal of the solvent by distillation gave the single compound, benzyl dithiobenzoate (2.22 g, 91%). It was further characterized by1H and 13C-NMR.
- A mixture of 4-methoxybenzoic acid (1.52 g), benzyl mercaptan (1.24 g) and phosphorus pentasulfide (4.44 g) in toluene (40 ml) was refluxed for 12 h. A dark red color was developed immediately after heating. After the reaction was complete (as monitored by GC-MS), it was cooled to room temperature and purified by a column chromatography packed with neutral alumina, eluting with benzene. Removal of the solvent by distillation gave the single compound, benzyl-4-methoxydithiobenzoate (1.89 g, 69%). It was further characterized by1H and 13C-NMR.
- A mixture of 4-fluorobenzoic acid (1.40 g), benzyl mercaptan (1.24 g) and phosphorus pentasulfide (4.44 g) in toluene (40 ml) was refluxed for 12 h. A dark red color was developed immediately after heating. After the reaction was complete (as monitored by GC-MS), it was cooled to room temperature and purified by a column chromatography packed with neutral alumina, eluting with benzene. Removal of the solvent by distillation gave the single compound, benzyl-4-fluorodithiobenzoate (1.86 g, 71%). It was further characterized by1H and 13C-NMR.
- A mixture of 4-nitrobenzoic acid (1.67 g), benzyl mercaptan (1.24 g) and phosphorus pentasulfide (4.44 g) in toluene (40 ml) was refluxed for 20 h. A dark red color was developed immediately after heating. After the reaction was complete (as monitored by GC-MS), it was cooled to room temperature and purified by a column chromatography packed with neutral alumina, eluting with benzene. Removal of the solvent by distillation gave the single compound, benzyl-4-nitrodithiobenzoate (1.48 g, 51%). It was further characterized by1H and 13C-NMR.
- A mixture of 4 cyanobenzoic acid (1.47 g), benzyl mercaptan (1.24 g) and phosphorus pentasulfide (4.44 g) in toluene (40 ml) was refluxed for 20 h. A dark red color was developed immediately after heating. After the reaction was complete (as monitored by GC-MS), it was cooled to room temperature and purified by a column chromatography packed with neutral alumina, eluting with benzene. Removal of the solvent by distillation gave the single compound, benzyl-4-cyanodithiobenzoate (1.15 g, 43%). It was further characterized by1H and 13C-NMR.
- A mixture of 4-trifluoromethylbenzoic acid (1.90 g), benzyl mercaptan (1.24 g) and phosphorus pentasulfide (4.44 g) in toluene (40 ml) was refluxed for 10 h. A dark red color was developed immediately after heating. After the reaction was complete (as monitored by GC-MS), it was cooled to room temperature and purified by a column chromatography packed with neutral alumina, eluting with benzene. Removal of the solvent by distillation gave the single compound, benzyl-4-trifluoromethyldithiobenzoate (2.30 g, 74%). It was further characterized by1H and 13C-NMR.
- A mixture of benzoic acid (1.22 g), thiophenol (1.10 g) and phosphorus pentasulfide (4.44 g) in toluene (40 ml) was refluxed for 8 h. A dark red color was developed immediately after heating. After the reaction was complete (as monitored by GC-MS), it was cooled to room temperature and purified by a column chromatography packed with neutral alumina, eluting with benzene. Removal of the solvent by distillation gave the single compound, diphenyl dithiobenzoate (1.56 g, 68%). It was further characterized by1H and 13C-NMR.
- A mixture of benzoic acid (1.22 g), 1-propanethiol (0.76 g) and phosphorus pentasulfide (4.44 g) in toluene (40 ml) was refluxed for 10 h. A dark red color was developed immediately after heating. After the reaction was complete (as monitored by GC-MS), it was cooled to room temperature and purified by a column chromatography packed with neutral alumina, eluting with benzene. Removal of the solvent by distillation gave the single compound, propyl dithiobenzoate (1.21 g, 62%). It was further characterized by1H and 13C-NMR.
- A mixture of propionic acid (0.74 g), benzyl mercaptan (1.24 g) and phosphorus pentasulfide (4.44 g) in toluene (40 ml) was refluxed for 10 h. A dark red color was developed immediately after heating. After the reaction was complete (as monitored by GC-MS), it was cooled to room temperature and purified by a column chromatography packed with neutral alumina, eluting with benzene. Removal of the solvent by distillation gave the desired compound, benzyl dithiopropionate (0.98 g, 50%) without further purification. The structure was confirmed by1H and 13C-NMR.
- A mixture of benzoic acid (1.22 g), benzyl alcohol (1.08 g) and phosphorus pentasulfide (4.44 g) in benzene (40 ml) was refluxed for 10 h. A dark red color was developed immediately after heating. After the reaction was complete (as monitored by GC-MS), it was cooled to room temperature and purified by a column chromatography packed with neutral alumina, eluting with benzene. Removal of the solvent by distillation gave the desired compound, benzyl dithiobenzoate (1.70 g, 70%) without further purification. The structure was confirmed by1H and 13C-NMR.
- A mixture of 4-methoxybenzoic acid (1.52 g), benzyl alcohol (1.08 g) and phosphorus pentasulfide (4.44 g) in benzene(40 ml) was refluxed for 12 h. A dark red color was developed immediately after heating. After the reaction was complete (as monitored by GC-MS), it was cooled to room temperature and purified by a column chromatography packed with neutral alumina, eluting with benzene. Removal of the solvent by distillation gave the required compound, benzyl-4-methoxydithiobenzoate (1.69 g, 62%) as the major product. The structure was confirmed by1H- and 13C-NMR.
- A mixture of 4-fluorobenzoic acid (1.40 g), benzyl alcohol (1.08 g) and phosphorus pentasulfide (4.44 g) in benzene (40 ml) was refluxed for 12 h. A dark red color was developed immediately after heating. After the reaction was complete (as monitored by GC-MS), it was cooled to room temperature and purified by a column chromatography packed with neutral alumina, eluting with benzene. Removal of the solvent by distillation gave the required compound, benzyl-4-fluorodithiobenzoate (1.36 g, 52%) without further purification. The structure was confirmed by1H and 13C-NMR.
- A mixture of 4-nitrobenzoic acid (1.67 g), benzyl alcohol (1.08 g) and phosphorus pentasulfide (4.44 g) in benzene (40 ml) was refluxed for 20 h. A dark red color was developed immediately after heating. After the reaction was complete (as monitored by GC-MS), it was cooled to room temperature and purified by a column chromatography packed with neutral alumina, eluting with benzene. Removal of the solvent by distillation gave the desired compound, benzyl-4-chlorodithiobenzoate (1.83 g, 66%) without further purification. The structure was confirmed by1H and 13C-NMR.
- A 50-ml round bottomed flask under nitrogen atmosphere was charged with 20 g of benzene, 100 mg of Montmorillonite (K-10) clay as catalyst 0.75 g of freshly distilled styrene and 1 g of thiobenzoic acid. The whole mixture was degassed with nitrogen for 15 minutes. The heterogeneous mixture was heated to reflux over the course of 10 minutes. The thiobenzoic acid conversion was determined at various times by GC-MS. The unreacted thiobenzoic acid was washed off completely using aqueous base (NaHCO3). The resulting product was analyzed by GC-MS, 1 H and 13C NMR. The conversion of thiobenzoic acid after 1440 minutes was 70% and the selectivity for the product 1 and 2 was 75% and 5% respectively.
- A 50-ml round bottomed flask under nitrogen atmosphere was charged with 20 g of benzene, 100 mg of Montmorillonite (KSF) clay as catalyst, 0.75 g of freshly distilled styrene and 1 g of thiobenzoic acid. The whole mixture was degassed with nitrogen for 15 minutes. The heterogeneous mixture was heated to reflux over the course of 10 minutes. The thiobenzoic acid conversion was determined by GC-MS. The unreacted thiobenzoic acid was washed off completely using aqueous base (NaHCO3). The resulting product was analyzed by GC-MS, 1 H and 13C NMR. The conversion of thiobenzoic acid after 1440 minutes was 78% and the selectivity for the product 1 and 2 was 49% and 29% respectively.
- A 50-ml round bottomed flask under nitrogen atmosphere was charged with 20 g of benzene, 100 mg of Montmorillonite (K-10) clay as catalyst, 0.75 g of styrene and 1 g of thiobenzoic acid. The whole mixture was degassed with nitrogen for 15 minutes. The heterogeneous mixture was stirred at room temperature for 960 minutes. The thiobenzoic acid conversion was determined by GC-MS. The unreacted thiobenzoic acid was washed off completely using aqueous base (NaHCO3). The resulting product was analyzed by GC-MS, 1H and 13C NMR. The conversion of thiobenzoic acid after 960 minutes was 94% and the selectivity for the product 1 and 2 was 6% and 76% respectively.
- A 50-ml round bottomed flask under nitrogen atmosphere was charged with 20 g of benzene, 100 mg of Montmorillonite (K-10) clay as catalyst, 0.86 g of p-methylstyrene and 1 g of thiobenzoic acid. The whole mixture was degassed with nitrogen for 15 minutes. The heterogeneous mixture was heated to reflux over the course of 10 minutes. The thiobenzoic acid conversion was determined by GC-MS. The unreacted thiobenzoic acid was washed off completely using aqueous base (NaHCO3). The resulting product was analyzed by GC-MS, 1 H and 13C NMR. The conversion of thiobenzoic acid after 960 minutes was 76% and the selectivity for the product 3 and 4 was 41% and 25% respectively.
- A 50-ml round bottomed flask under nitrogen atmosphere was charged with 20 g of benzene, 100 mg of Montmorillonite (K-10) clay as catalyst, 0.86 g of α-methylstyrene and 1 g of thiobenzoic acid. The mixture was degassed with nitrogen for 15 minutes. The heterogeneous mixture was heated to reflux over the course of 10 minutes. The thiobenzoic acid conversion was determined by GC-MS. The unreacted thiobenzoic acid was washed off completely using aqueous base (NaHCO3). The resulting product was analyzed by GC-MS, 1 H and 13C NMR. The conversion of thiobenzoic acid after 960 minutes was 80% and the selectivity for the product 5 and 6 was 76% and 3% respectively.
- A 50-ml round bottomed flask under nitrogen atmosphere was charged with 20 g of benzene, 100 mg of Montmorillonite (K-10) clay as catalyst, 0.58 g of 1-hexene and 1 g of thiobenzoic acid. The whole mixture was degassed with nitrogen for 15 minutes. The heterogeneous mixture was heated to reflux over the course of 10 minutes. The thiobenzoic acid conversion was determined by GC-MS. The unreacted thiobenzoic acid was washed off completely using aqueous base (NaHCO3). The resulting product was analyzed by GC-MS, 1 H and 13C NMR. The conversion of thiobenzoic acid after 960 minutes was 85% and the selectivity for products 7 and 8 was 65% and 20% respectively.
- A 50-ml round bottomed flask under nitrogen atmosphere was charged with 20 g of benzene, 100 mg of Montmorillonite (K-10) clay as catalyst, 0.72 g of MMA and 1 g of thiobenzoic acid. The whole mixture was degassed with nitrogen for 15 minutes. The heterogeneous mixture was heated to reflux over the course of 10 minutes. The thiobenzoic acid conversion was determined by GC-MS. The unreacted thiobenzoic acid was washed off completely using aqueous base (NaHCO3). The resulting product was analyzed by GC-MS, 1 H and 13C NMR. The conversion of thiobenzoic acid after 960 minutes was 96% and the selectivity for products 9 and 10 was 58% and 14% respectively.
- A 25-ml round bottomed flask under nitrogen atmosphere was charged with 10 g of toluene, 500 mg Lawesson's reagent and 450 mg of structure 1. The whole mixture was degassed with nitrogen for 15 minutes. The mixture was heated to reflux over the course of 10 minutes and continued for 2 hrs. The crude product was purified by passing through neutral alumna. The resulting product was analyzed by GC-MS, 1 H and 13C NMR. The yield of dithicarboxylic acid of structure II was 95%.
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