CN109251217B - Application of o-methoxyanilino lithium in catalysis of imine and borane hydroboration reaction - Google Patents
Application of o-methoxyanilino lithium in catalysis of imine and borane hydroboration reaction Download PDFInfo
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- UORVGPXVDQYIDP-UHFFFAOYSA-N borane Chemical compound B UORVGPXVDQYIDP-UHFFFAOYSA-N 0.000 title claims abstract description 62
- 229910000085 borane Inorganic materials 0.000 title claims abstract description 31
- 150000002466 imines Chemical class 0.000 title claims abstract description 31
- 238000006197 hydroboration reaction Methods 0.000 title claims abstract description 29
- AVYWQIYILZLMII-UHFFFAOYSA-N lithium;(2-methoxyphenyl)azanide Chemical compound [Li+].COC1=CC=CC=C1[NH-] AVYWQIYILZLMII-UHFFFAOYSA-N 0.000 title claims abstract description 24
- 238000006555 catalytic reaction Methods 0.000 title description 2
- 238000006243 chemical reaction Methods 0.000 claims abstract description 36
- 239000003054 catalyst Substances 0.000 claims abstract description 15
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical group C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims description 45
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 claims description 22
- LZPWAYBEOJRFAX-UHFFFAOYSA-N 4,4,5,5-tetramethyl-1,3,2$l^{2}-dioxaborolane Chemical group CC1(C)O[B]OC1(C)C LZPWAYBEOJRFAX-UHFFFAOYSA-N 0.000 claims description 17
- 230000018044 dehydration Effects 0.000 claims description 16
- 238000006297 dehydration reaction Methods 0.000 claims description 16
- 238000000034 method Methods 0.000 claims description 5
- 239000003960 organic solvent Substances 0.000 claims description 5
- 239000011261 inert gas Substances 0.000 claims description 3
- 239000000126 substance Substances 0.000 claims description 3
- 125000006575 electron-withdrawing group Chemical group 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical class 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- GRVDJDISBSALJP-UHFFFAOYSA-N methyloxidanyl Chemical group [O]C GRVDJDISBSALJP-UHFFFAOYSA-N 0.000 claims 1
- -1 borate ester Chemical class 0.000 abstract description 18
- 230000003197 catalytic effect Effects 0.000 abstract description 7
- 230000000694 effects Effects 0.000 abstract description 2
- 239000002904 solvent Substances 0.000 abstract description 2
- 125000001424 substituent group Chemical group 0.000 abstract 2
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 238000003756 stirring Methods 0.000 abstract 1
- HEDRZPFGACZZDS-MICDWDOJSA-N deuterated chloroform Substances [2H]C(Cl)(Cl)Cl HEDRZPFGACZZDS-MICDWDOJSA-N 0.000 description 37
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 26
- 229910052744 lithium Inorganic materials 0.000 description 18
- 238000005160 1H NMR spectroscopy Methods 0.000 description 13
- 229910052786 argon Inorganic materials 0.000 description 13
- 238000001228 spectrum Methods 0.000 description 13
- UVEWQKMPXAHFST-UHFFFAOYSA-N n,1-diphenylmethanimine Chemical compound C=1C=CC=CC=1C=NC1=CC=CC=C1 UVEWQKMPXAHFST-UHFFFAOYSA-N 0.000 description 8
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 4
- 230000035484 reaction time Effects 0.000 description 3
- CFBVFBIZXQEQHX-UHFFFAOYSA-N 1-(4-chlorophenyl)-n-phenylmethanimine Chemical compound C1=CC(Cl)=CC=C1C=NC1=CC=CC=C1 CFBVFBIZXQEQHX-UHFFFAOYSA-N 0.000 description 2
- MPRONVWLCPZXOB-UHFFFAOYSA-N 1-(4-fluorophenyl)-n-phenylmethanimine Chemical compound C1=CC(F)=CC=C1C=NC1=CC=CC=C1 MPRONVWLCPZXOB-UHFFFAOYSA-N 0.000 description 2
- 125000003277 amino group Chemical group 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- DJGDQBWKJYPZEF-UHFFFAOYSA-N n-(4-bromophenyl)-1-phenylmethanimine Chemical compound C1=CC(Br)=CC=C1N=CC1=CC=CC=C1 DJGDQBWKJYPZEF-UHFFFAOYSA-N 0.000 description 2
- NWCAQYVAHZWHIO-UHFFFAOYSA-N n-(4-chlorophenyl)-1-phenylmethanimine Chemical compound C1=CC(Cl)=CC=C1N=CC1=CC=CC=C1 NWCAQYVAHZWHIO-UHFFFAOYSA-N 0.000 description 2
- MJSLSMOBYCYMIM-UHFFFAOYSA-N 1-(4-bromophenyl)-n-phenylmethanimine Chemical compound C1=CC(Br)=CC=C1C=NC1=CC=CC=C1 MJSLSMOBYCYMIM-UHFFFAOYSA-N 0.000 description 1
- PCICJNSIYHONRK-UHFFFAOYSA-N 1-(4-methylphenyl)-n-phenylmethanimine Chemical compound C1=CC(C)=CC=C1C=NC1=CC=CC=C1 PCICJNSIYHONRK-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 150000004705 aldimines Chemical group 0.000 description 1
- 229930013930 alkaloid Natural products 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 229940088710 antibiotic agent Drugs 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910003002 lithium salt Inorganic materials 0.000 description 1
- 159000000002 lithium salts Chemical class 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- KDKHRAVKGIIQHF-UHFFFAOYSA-N methyl n-phenylbenzenecarboximidate Chemical compound C=1C=CC=CC=1C(OC)=NC1=CC=CC=C1 KDKHRAVKGIIQHF-UHFFFAOYSA-N 0.000 description 1
- OEJZOCTWYUFFNN-UHFFFAOYSA-N n-(4-fluorophenyl)-1-phenylmethanimine Chemical compound C1=CC(F)=CC=C1N=CC1=CC=CC=C1 OEJZOCTWYUFFNN-UHFFFAOYSA-N 0.000 description 1
- MSFVFFZPHJPOHP-UHFFFAOYSA-N n-(4-methylphenyl)-1-phenylmethanimine Chemical compound C1=CC(C)=CC=C1N=CC1=CC=CC=C1 MSFVFFZPHJPOHP-UHFFFAOYSA-N 0.000 description 1
- UFSVSYSCODIMCX-UHFFFAOYSA-N n-[(4-bromophenyl)methyl]aniline Chemical compound C1=CC(Br)=CC=C1CNC1=CC=CC=C1 UFSVSYSCODIMCX-UHFFFAOYSA-N 0.000 description 1
- 102000039446 nucleic acids Human genes 0.000 description 1
- 108020004707 nucleic acids Proteins 0.000 description 1
- 150000007523 nucleic acids Chemical class 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 230000001766 physiological effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 239000004753 textile Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
- C07F5/02—Boron compounds
- C07F5/022—Boron compounds without C-boron linkages
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
- B01J31/0234—Nitrogen-, phosphorus-, arsenic- or antimony-containing compounds
- B01J31/0235—Nitrogen containing compounds
- B01J31/0252—Nitrogen containing compounds with a metal-nitrogen link, e.g. metal amides, metal guanidides
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
Abstract
The invention relates to application of o-methoxyanilino lithium, in particular to application of o-methoxyanilino lithium in catalyzing hydroboration reaction of imine and borane. And stirring and mixing the catalyst, borane and imine uniformly in sequence, reacting for 1-2 hours, exposing the mixture to air to terminate the reaction, and decompressing the reaction solution to remove the solvent to obtain the borate with different substituent groups. The o-methoxyanilino lithium disclosed by the invention can catalyze the hydroboration reaction of imine and borane with high activity at room temperature, the dosage of the catalyst is only 4-5 mol% of the molar weight of imine, the reaction yield can reach more than 90%, compared with the existing catalytic system, the o-methoxyanilino lithium is utilized, the reaction condition is mild, and the yield of borate ester with different substituents under the optimized condition can reach 99%.
Description
Technical Field
The invention relates to application of o-methoxyanilino lithium, in particular to efficient application of the o-methoxyanilino lithium in catalyzing hydroboration reaction of imine and borane.
Technical Field
The amine compounds and derivatives thereof are ubiquitous in nature, especially widely exist in the biological world, and have extremely important physiological effects. They are important organic compounds in the fields of biology, chemistry, medicine, etc., and many drugs contain amine functional groups, i.e., amino groups, such as those found in proteins, nucleic acids, antibiotics, and alkaloids. The amine compound has various use values and wide application range, and is often used for synthesizing textiles, dyes, polymers, pigments, pesticides and the like. Since the hydroboration reaction of carbonyl is far easier to occur than that of imine, a high-efficiency catalytic system for the hydroboration reaction of unsaturated C = N bond is developed, and the method has important significance for modern industry and organic synthetic chemistry.
The hydroboration reaction of imine has become a research hotspot in recent years, and the reported catalyst applied to the hydroboration reaction of imine mainly comprises a catalytic system of main group elements: magnesium [ Manna, K.; Ji, P.; Greene, F. X.; Lin, W.J. Am. chem. Soc. 2016, 138, 7488-; however, the catalyst systems reported at present are relatively expensive or difficult to prepare, or have long reaction time and are required to react at high temperature, and some catalytic systems have low yield. Therefore, it is very important to develop a catalytic system for efficiently catalyzing the hydroboration reaction of imine under mild conditions.
Disclosure of Invention
The invention aims to provide application of o-methoxyanilino lithium, namely application of o-methoxyanilino lithium serving as a high-efficiency catalyst for catalyzing imine and borane to undergo hydroboration reaction.
The invention discloses simple lithium o-methoxyanilino for the first time, which can catalyze the hydroboration reaction of imine under mild reaction conditions, has high yield and wide substrate application range. Cheap catalyst and mild catalytic condition, and provides possibility for industrial application. In order to achieve the purpose of the invention, the technical scheme adopted by the invention is as follows:
the application of o-methoxyanilino lithium in catalyzing the hydroboration reaction of imine and borane; the chemical formula of the o-methoxyanilino lithium is 2-OCH3PhNHLi。
The invention also discloses a method for catalyzing imine and borane to perform hydroboration reaction by using the lithium o-methoxyanilino, which comprises the following steps: under the anhydrous and oxygen-free environment and in the inert gas atmosphere, adding imine into a reaction bottle subjected to dehydration and deoxidation treatment, adding an organic solvent, then adding borane, uniformly mixing, adding a catalyst of o-methoxyanilino lithium, reacting for 1-2 h, and exposing in the air to terminate the reaction to obtain a product.
The invention also discloses a method for preparing boric acid ester by carrying out hydroboration reaction on imine and borane, which comprises the following steps: under the anhydrous and oxygen-free environment and in the inert gas atmosphere, adding imine into a reaction bottle subjected to dehydration and deoxidation treatment, adding an organic solvent, then adding borane, uniformly mixing, adding a catalyst of o-methoxyanilino lithium, reacting for 1-2 h, and exposing in the air to terminate the reaction to obtain a product.
In the above technical scheme, the imine is selected from aldimine; the chemical structural general formula of the imine is as follows:
wherein R is1Or R2Is one of electron withdrawing group or electron donating group, and can be selected from halogen, methyl and methoxy; the borane is selected from pinacol borane.
In the technical scheme, the using amount of the catalyst can be 4-5% of the mole number of the imine, and the mole ratio of the imine to the pinacol borane is 1: 1-1: 1.2.
In the technical scheme, the reaction temperature is room temperature, and the reaction time is 1-2 h.
In the above technical scheme, the organic solvent is tetrahydrofuran.
The above technical solution can be expressed as follows:
due to the application of the technical scheme, compared with the prior art, the invention has the following advantages:
1. the invention discovers for the first time that the simple lithium salt of o-methoxyanilino can efficiently catalyze imine and borane to carry out hydroboration reaction, and the method is highly suitable for atom economic synthesis.
2. The o-methoxyanilino lithium catalyst disclosed by the invention has the advantages of high catalytic activity (the dosage of the catalyst can be 4-5% of the mole number of the imine), mild reaction conditions (room temperature), short reaction time (1-2 h), high reaction yield, simple and controllable reaction, simple post-treatment and low-cost THF (tetrahydrofuran) adopted as a solvent in the reaction.
3. The catalyst disclosed by the invention has better universality for imines with different substitution positions and different electronic effects.
Detailed Description
The invention is further described below with reference to examples:
the first embodiment is as follows: lithium o-methoxyanilino group for catalyzing hydroboration reaction of benzylidene aniline and pinacol borane
Adding 0.5 mmol of benzylidene aniline into a reaction bottle subjected to dehydration and deoxidation treatment under the protection of argon, adding 100 ul of THF, adding 0.5 mmol (0.0726 mL) of borane into a liquid-transferring gun, uniformly mixing, finally adding 39.2 ul of tetrahydrofuran solution (0.6387M) of o-methoxyanilino lithium (5 mol% dosage, the same below), reacting for 2 h, sucking a drop of nuclear magnetic tube by a dropper, adding CDCl3Preparing a solution. Is calculated by1The yield by H spectrum was 91%. Nuclear magnetic data of the product:1H NMR (CDCl3, 400 MHz) δ: 7.29~7.12(m, 9H), 6.88~6.84 (t, 1H), 4.69 (s, 1H), 1.29 (s, 12H)。
example II lithium o-methoxyanilino catalyzed hydrogenation of benzylidene aniline with pinacol borane
Adding 0.5 mmol of benzylidene aniline into a reaction bottle subjected to dehydration and deoxidation treatment under the protection of argon, adding 100 ul of THF, adding 0.6 mmol (0.0871 mL) of borane into a liquid-transferring gun, uniformly mixing, finally adding 39.2 ul of tetrahydrofuran solution (0.6387M) of o-methoxyanilino lithium (5 mol% dosage, the same below), reacting for 1h, sucking a drop of nuclear magnetic tube by a dropper, adding CDCl3Preparing a solution. Warp gaugeCalculating out1The yield of the H spectrum is 96%. Nuclear magnetic data of the product:1H NMR (CDCl3, 400 MHz) δ: 7.29~7.12(m, 9H), 6.88~6.84 (t, 1H), 4.69 (s, 2H), 1.29 (s, 12H)。
example three: lithium o-methoxyanilino group for catalyzing hydroboration reaction of benzylidene aniline and pinacol borane
Adding 0.5 mmol of benzylidene aniline into a reaction bottle subjected to dehydration and deoxidation treatment under the protection of argon, adding 100 ul of THF, adding 0.6 mmol (0.0871 mL) of borane into a liquid-transferring gun, uniformly mixing, finally adding 39.2 ul of tetrahydrofuran solution (0.6387M) (5 mol% dosage) of o-methoxyanilino lithium, absorbing one drop of solution into a nuclear magnetic tube by a dropper after reacting for 2 hours, and adding CDCl3Preparing a solution. Is calculated by1The yield of the H spectrum is 99%. Nuclear magnetic data of the product:1H NMR (CDCl3, 400 MHz) δ: 7.29~7.12(m, 9H), 6.88~6.84 (t, 1H), 4.69 (s, 2H), 1.29 (s, 12H)。
the product cannot be obtained by replacing lithium o-methoxyanilino with an aminolithium compound of formula I.
Example four: lithium o-methoxyanilino group for catalyzing hydroboration reaction of benzylidene aniline and pinacol borane
Adding 0.5 mmol of benzylidene aniline into a reaction bottle subjected to dehydration and deoxidation treatment under the protection of argon, adding 100 ul of THF, adding 0.6 mmol (0.0871 mL) of borane into a liquid-transferring gun, uniformly mixing, finally adding 31.3 ul of tetrahydrofuran solution (0.6387M) (4 mol% dosage) of o-methoxyanilino lithium, absorbing one drop of solution into a nuclear magnetic tube by a dropper after reacting for 2 hours, and adding CDCl3Preparing a solution. Is calculated by1The yield of the H spectrum is 97%. Nuclear magnetic data of the product:1H NMR (CDCl3, 400 MHz) δ: 7.29~7.12(m, 9H), 6.88~6.84 (t, 1H), 4.69 (s, 2H), 1.29 (s, 12H)。
example five: lithium o-methoxyanilino as catalyst for N-, (p-methylbenzylidene) aniline with pinacolborane borohydrideChemical reaction
Adding 0.5 mmol of N-, (N) into a reaction bottle subjected to dehydration and deoxidation treatment under the protection of argonp-methylbenzylidene) aniline, 100 ul THF, 0.6 mmol (0.0871 mL) borane by means of a pipette, mixing homogeneously, finally 39.2 ul of a solution of lithium o-methoxyanilino in tetrahydrofuran (0.6387M) (5 mol% amount, the same applies hereinafter) are added, after 2 h of reaction, one drop is pipetted into a nuclear magnetic tube and CDCl is added3Preparing a solution. Is calculated by1The yield of the H spectrum is 99%. Nuclear magnetic data of the product:1H NMR (CDCl3, 400 MHz) δ: 7.23~7.08(m, 8H), 6.89~6.85 (t, 1H), 4.66 (s, 2H), 2.31 (s, 3H), 1.30 (s, 12H)。
example six: lithium o-methoxyanilino as catalyst for N-, (pHydroboration of (methoxybenzylidene) aniline with pinacol borane
Adding 0.5 mmol of N-, (N) into a reaction bottle subjected to dehydration and deoxidation treatment under the protection of argonp-methoxybenzylidene) aniline, 100 ul THF, 0.6 mmol (0.0871 mL) borane by pipette, and finally 39.2 ul lithium o-methoxyanilino in tetrahydrofuran (0.6387M) (5 mol% amount, the same applies below) are added, and after 2 h reaction, one drop of the compound is pipetted into a nuclear magnetic tube, and CDCl is added3Preparing a solution. Is calculated by1The yield of the H spectrum is 99%. Nuclear magnetic data of the product:1H NMR (CDCl3, 400 MHz) δ: 7.22~7.13(d, 6H), 6.89~6.80 (d, 3H), 4.63 (s, 2H), 3.77 (s, 3H), 1.30 (s, 12H)。
example seven: lithium o-methoxyanilino for hydroboration of N- (4-fluorobenzylidene) aniline and pinacol borane
Adding 0.5 mmol of N- (4-fluorobenzylidene) aniline into a reaction bottle subjected to dehydration and deoxidation treatment under the protection of argon, adding 100 ul of THF, then adding 0.6 mmol (0.0871 mL) of borane into a pipette gun, uniformly mixing, finally adding 39.2 ul of o-methoxyanilino lithium tetrahydrofuran solution (0.6387M) (5 mol% dosage, the same below) into the reaction bottle, reacting for 2 hours, absorbing the reaction bottle by a dropper into a nuclear magnetic tube, adding CDCl3Preparing a solution. Is calculated by1The yield of the H spectrum is 99%. Nuclear magnetic number of productAccording to the following steps:1H NMR (CDCl3, 400 MHz) δ: 7.22~7.15(d, 6H), 6.98~6.94 (d, 3H), 4.66 (s, 2H), 1.30 (s, 12H)。
example eight: lithium o-methoxyanilino for hydroboration of N- (4-chlorobenzylidene) aniline and pinacol borane
Adding 0.5 mmol of N- (4-chlorobenzylidene) aniline into a reaction bottle subjected to dehydration and deoxidation treatment under the protection of argon, adding 100 ul of THF, then adding 0.6 mmol (0.0871 mL) of borane into a pipette gun, uniformly mixing, finally adding 39.2 ul of o-methoxyanilino lithium tetrahydrofuran solution (0.6387M) (5 mol% dosage, the same below) into the reaction bottle, reacting for 2 hours, absorbing one drop by a dropper into a nuclear magnetic tube, adding CDCl3Preparing a solution. Is calculated by1The yield of the H spectrum is 99%. Nuclear magnetic data of the product:1H NMR (CDCl3, 400 MHz) δ: 7.20~7.14(d, 6H), 6.99~6.93 (d, 3H), 4.64 (s, 2H), 1.30 (s, 12H)。
example nine: lithium o-methoxyanilino for hydroboration of N- (4-bromobenzyl) aniline and pinacol borane
Adding 0.5 mmol of N- (4-bromobenzylidene) aniline into a reaction bottle subjected to dehydration and deoxidation treatment under the protection of argon, adding 100 ul of THF, then adding 0.6 mmol (0.0871 mL) of borane into a pipette gun, uniformly mixing, finally adding 39.2 ul of o-methoxyanilino lithium tetrahydrofuran solution (0.6387M) (5 mol% dosage, the same below), reacting for 2 hours, absorbing one drop by a dropper into a nuclear magnetic tube, adding CDCl3Preparing a solution. Is calculated by1The yield of the H spectrum is 99%. Nuclear magnetic data of the product:1H NMR (CDCl3, 400 MHz) δ: 7.24~7.16(d, 6H), 6.97~6.93 (d, 3H), 4.63 (s, 2H), 1.31 (s, 12H)。
example ten: lithium o-methoxyanilino for hydroboration of benzylidene-p-toluidine and pinacol borane
In a reaction bottle which is subjected to dehydration and deoxidation treatment, 0.5 mmol of benzylidene p-toluene is added under the protection of argon, 100 ul of THF is added, then 0.6 mmol (0.0871 mL) of borane is added by a pipette and mixed evenly, and finally 39.2 ul of tetrahydrofuran solution (0.6387) of o-methoxyanilino lithium is addedM) (5 mol% dosage, the same below) and reacting for 2 h, sucking one drop into a nuclear magnetic tube by a dropper, and adding CDCl3Preparing a solution. Is calculated by1The yield of the H spectrum is 99%. Nuclear magnetic data of the product:1H NMR (CDCl3, 400 MHz) δ: 7.32~7.28(d, 5H), 7.10~7.08 (d, 2H), 6.64~6.60 (d, 2H), 4.62 (s, 2H), 1.31 (s, 12H)。
example eleven: lithium o-methoxyanilino for catalyzing hydroboration reaction of N- (benzylidene) -4-fluoroaniline and pinacol borane
Adding 0.5 mmol of benzylidene p-toluene into a reaction bottle subjected to dehydration and deoxidation treatment under the protection of argon, adding 100 ul of THF, then adding 0.6 mmol (0.0871 mL) of borane into a liquid-transferring gun, uniformly mixing, finally adding 39.2 ul of o-methoxyanilino lithium tetrahydrofuran solution (0.6387M) (5 mol% dosage, the same below), reacting for 2 hours, sucking one drop by a dropper into a nuclear magnetic tube, adding CDCl3Preparing a solution. Is calculated by1The yield of the H spectrum is 99%. Nuclear magnetic data of the product:1H NMR (CDCl3, 400 MHz) δ: 7.24~7.02(d, 7H), 6.75~6.70 (d, 2H), 4.66 (s, 2H), 1.32 (s, 12H)。
example twelve: lithium o-methoxyanilino for catalyzing hydroboration reaction of N- (benzylidene) -4-chloroaniline and pinacol borane
Adding 0.5 mmol of N- (benzylidene) -4-chloroaniline into a reaction bottle subjected to dehydration and deoxidation treatment under the protection of argon, adding 100 ul of THF, then adding 0.6 mmol (0.0871 mL) of borane into a pipette gun, uniformly mixing, finally adding 39.2 ul of o-methoxyanilino lithium tetrahydrofuran solution (0.6387M) (5 mol% dosage, the same below), reacting for 2 hours, absorbing one drop by a dropper into a nuclear magnetic tube, adding CDCl3Preparing a solution. Is calculated by1The yield of the H spectrum is 99%. Nuclear magnetic data of the product:1H NMR (CDCl3, 400 MHz) δ: 7.26~7.05(d, 7H), 6.74~6.69 (d, 2H), 4.61 (s, 2H), 1.30 (s, 12H)。
example thirteen: lithium o-methoxyanilino for catalyzing hydroboration reaction of N- (benzylidene) -4-bromoaniline and pinacol borane
In a reaction bottle which is subjected to dehydration and deoxidation treatmentAdding 0.5 mmol of N- (benzylidene) -4-bromoaniline under the protection of argon, adding 100 ul of THF, adding 0.6 mmol (0.0871 mL) of borane by using a liquid transfer gun, uniformly mixing, finally adding 39.2 ul of an o-methoxyanilino lithium tetrahydrofuran solution (0.6387M) (4 mol% dosage, the same below), absorbing one drop in a nuclear magnetic tube by using a dropper after reacting for 2 hours, and adding CDCl3Preparing a solution. Is calculated by1The yield of the H spectrum is 99%. Nuclear magnetic data of the product:1H NMR (CDCl3, 400 MHz) δ: 7.27~7.03(d, 7H), 6.76~6.71 (d, 2H), 4.62 (s, 2H), 1.30 (s, 12H)。
Claims (1)
1. the application of the o-methoxyanilino lithium in catalyzing the hydroboration reaction of imine and borane is characterized in that the method for catalyzing the hydroboration reaction of imine and borane by the o-methoxyanilino lithium comprises the following steps: under the anhydrous and oxygen-free environment and the inert gas atmosphere, adding imine into a reaction bottle subjected to dehydration and deoxidation treatment, adding an organic solvent, then adding borane, uniformly mixing, adding a catalyst of o-methoxyanilino lithium, reacting at room temperature for 1-2 h, and exposing the reaction bottle to air to terminate the reaction to obtain a product; the chemical structural general formula of the imine is as follows:
wherein R is1Or R2Is one of electron withdrawing group or electron donating group, and is selected from halogen, methyl and methoxyl; the borane is selected from pinacol borane; the organic solvent is tetrahydrofuran;
the dosage of the o-methoxyanilino lithium is 4-5% of the mole number of the imine, and the mole ratio of the imine to the pinacol borane is 1: 1-1: 1.2.
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| CN108440589A (en) * | 2018-04-16 | 2018-08-24 | 苏州大学 | The method for preparing borate based on o-methyl-benzene amido lithium |
| CN108503660A (en) * | 2018-04-16 | 2018-09-07 | 苏州大学 | Application of the anilino- lithium in catalysis aldehyde and borine hydroboration |
| CN108554446A (en) * | 2018-04-16 | 2018-09-21 | 苏州大学 | Application of the open-chain crown ether base lithium in catalysis aldehyde and borine hydroboration |
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| CN108440589A (en) * | 2018-04-16 | 2018-08-24 | 苏州大学 | The method for preparing borate based on o-methyl-benzene amido lithium |
| CN108503660A (en) * | 2018-04-16 | 2018-09-07 | 苏州大学 | Application of the anilino- lithium in catalysis aldehyde and borine hydroboration |
| CN108554446A (en) * | 2018-04-16 | 2018-09-21 | 苏州大学 | Application of the open-chain crown ether base lithium in catalysis aldehyde and borine hydroboration |
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| Rhenium-catalysed hydroboration of aldehydes and aldimines;Rebeca Arévalo et al.;《Dalton Trans.》;20170530;第46卷;第7750-7757页 * |
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