GB944406A - New cyclic sulphurous and sulphuric esters and methods of preparing the same - Google Patents

New cyclic sulphurous and sulphuric esters and methods of preparing the same

Info

Publication number
GB944406A
GB944406A GB2435159A GB2435159A GB944406A GB 944406 A GB944406 A GB 944406A GB 2435159 A GB2435159 A GB 2435159A GB 2435159 A GB2435159 A GB 2435159A GB 944406 A GB944406 A GB 944406A
Authority
GB
United Kingdom
Prior art keywords
saturated
aliphatic hydrocarbon
aralkyl group
unsaturated aliphatic
aryl
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB2435159A
Inventor
Leslie Frederick Wiggins
Colin Charles Beard
John William James
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Aspro Nicholas Ltd
Original Assignee
Aspro Nicholas Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Aspro Nicholas Ltd filed Critical Aspro Nicholas Ltd
Priority to GB2435159A priority Critical patent/GB944406A/en
Publication of GB944406A publication Critical patent/GB944406A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D327/00Heterocyclic compounds containing rings having oxygen and sulfur atoms as the only ring hetero atoms
    • C07D327/10Heterocyclic compounds containing rings having oxygen and sulfur atoms as the only ring hetero atoms two oxygen atoms and one sulfur atom, e.g. cyclic sulfates

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)

Abstract

The invention comprises compounds of the general formula: <FORM:0944406/C2/1> wherein (A) when m is 1 and n is zero, R1 is a hydrogen atom, a C1-8 saturated or unsaturated aliphatic hydrocarbon or an aryl or aralkyl group, R2 is a C1-8 saturated aliphatic hydrocarbon or an aryl or aralkyl group, and R3 and R4 are each hydrogen atoms or C1-8 saturated or unsaturated aliphatic hydrocarbon groups or aralkyl groups; (B) when m is 1 and n is 1, either (a) R1 and R2 are both hydrogen atoms, in which case R3 is a C1-8 saturated or unsaturated aliphatic hydrocarbon or an aralkyl group, and R4 is a C2-8 saturated or unsaturated aliphatic hydrocarbon, an aryl or an aralkyl group, or (b) R3 and R4 are both hydrogen atoms, in which case R1 and R2 are each a C2-8 saturated or unsaturated aliphatic hydrocarbon group or an aryl or aralkyl group; and (c) when m is 2 and n is zero or 1, R1 and R2 are each a hydrogen atom, or a C1-8 saturated or unsaturated aliphatic hydrocarbon, an aryl or an aralkyl group and R3 and R4 are each a C1-8 saturated or unsaturated aliphatic hydrocarbon, an aryl or an aralkyl group, and the preparation thereof (a) (when m is 1 and n is zero or 1) by treating an appropriate diol with an excess of thionyl chloride with or without an inert solvent, heating the resulting mixture under reflux, and thereafter removing excess thionyl chloride and solvent, if used, to obtain the desired ester; or by reacting the appropriate diol with an exact equivalent of thionyl chloride in an inert solvent, with or without heat, thereafter removing the solvent to obtain the desired ester, or by reacting a mixture of the appropriate diol, a base and an inert solvent with thionyl chloride, preferably at between -20 DEG and -30 DEG C., and thereafter recovering the desired ester from the reaction mixture; or (b) (when m is 2 and n is zero or 1) by oxidising the corresponding sulphurous acid ester in an appropriate solvent with an oxidising agent.
GB2435159A 1959-07-15 1959-07-15 New cyclic sulphurous and sulphuric esters and methods of preparing the same Expired GB944406A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2435159A GB944406A (en) 1959-07-15 1959-07-15 New cyclic sulphurous and sulphuric esters and methods of preparing the same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2435159A GB944406A (en) 1959-07-15 1959-07-15 New cyclic sulphurous and sulphuric esters and methods of preparing the same

Publications (1)

Publication Number Publication Date
GB944406A true GB944406A (en) 1963-12-11

Family

ID=10210348

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2435159A Expired GB944406A (en) 1959-07-15 1959-07-15 New cyclic sulphurous and sulphuric esters and methods of preparing the same

Country Status (1)

Country Link
GB (1) GB944406A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5171892A (en) * 1991-07-02 1992-12-15 E. I. Du Pont De Nemours And Company Chiral phospholanes via chiral 1,4-diol cyclic sulfates

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5171892A (en) * 1991-07-02 1992-12-15 E. I. Du Pont De Nemours And Company Chiral phospholanes via chiral 1,4-diol cyclic sulfates
US5329015A (en) * 1991-07-02 1994-07-12 E. I. Du Pont De Nemours And Company Chiral phospholanes via chiral 1,4-diol cyclic sulfates
US5532395A (en) * 1991-07-02 1996-07-02 E. I. Du Pont De Nemours And Company Chiral phospholanes via chiral 1,4-diol cyclic sulfates
US5559267A (en) * 1991-07-02 1996-09-24 E. I. Du Pont De Nemours And Company Hydrogenation process using catalysts made from chiral phospholanes via chiral 1,4-diol cyclic sulfates
US5565593A (en) * 1991-07-02 1996-10-15 E. I. Du Pont De Nemours And Company Chiral phospholanes via chiral 1,4-diol cyclic sulfates
US5596114A (en) * 1991-07-02 1997-01-21 E. I. Du Pont De Nemours And Company Chiral phospholanes via chiral 1 4-diol cyclic sulfates

Similar Documents

Publication Publication Date Title
GB1526410A (en) 4-(e)-and 4-(z)-7-methyl-9-(2,6,6-trimethyl-1-cyclohexen-1-yl)-nona-2,4,6,8-tetraenecarboxylic acid their derivatives and preparations containing same
GB1070323A (en) Process for the preparation of epsilon-caprolactones
Goering et al. The Solvolysis of cis-and trans-2-Chlorocycloalkyl Aryl Sulfides in 80% Aqueous Ethanol1
GB1033777A (en) Bis-anilide derivatives
GB944406A (en) New cyclic sulphurous and sulphuric esters and methods of preparing the same
GB977071A (en) Hydroxylamine derivatives and process for making them
FR1166782A (en) Manufacturing process of toluic acid chloride
GB1069485A (en) Process for producing anthraquinone disperse dyestuffs
ES434460A1 (en) Process for the production of aromatic and cycloaliphatic dicarboxylic acid diamides
US2750390A (en) Nicotinic acid ester
GB1048989A (en) 2-chloro-s-triazines
GB867268A (en) Process for preparing 3-nitro-azacyclo-alkanone-2-n-carbochlorides
GB893923A (en) Movements in or relating to steroids and the manufacture thereof
GB910262A (en) New nicotinic acid esters and methods of producing them
SE7501801L (en)
GB1056936A (en) Novel pregnane compounds and processes for their preparation
GB1001830A (en) Novel indeno-[5,4-e]-azulene derivatives and processes for the preparation thereof
ES405907A1 (en) O-alkyl-o-cyclohexyl-s-alkyl-,haloalkyl-or alkenyl-phosphorothiolates
GB938445A (en) Improvements in or relating to steroids
GB908628A (en) New nicotinic acid esters and methods of producing them
ES298219A1 (en) A procedure for preparing new steroid compounds (Machine-translation by Google Translate, not legally binding)
GB957954A (en) Steroids and their production
GB939510A (en) Process for the manufacture of pregnadienes
GB779001A (en) Steroid 3-enamines
GB955352A (en) Method of preparing polynitro compounds