GB1010491A - Improvements relating to the production of aryl alkyl sulphones - Google Patents

Improvements relating to the production of aryl alkyl sulphones

Info

Publication number
GB1010491A
GB1010491A GB3372862A GB3372862A GB1010491A GB 1010491 A GB1010491 A GB 1010491A GB 3372862 A GB3372862 A GB 3372862A GB 3372862 A GB3372862 A GB 3372862A GB 1010491 A GB1010491 A GB 1010491A
Authority
GB
United Kingdom
Prior art keywords
sulphone
aryl alkyl
excess
aromatic
production
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
GB3372862A
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.)
Centre National de la Recherche Scientifique CNRS
Original Assignee
Centre National de la Recherche Scientifique CNRS
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 Centre National de la Recherche Scientifique CNRS filed Critical Centre National de la Recherche Scientifique CNRS
Publication of GB1010491A publication Critical patent/GB1010491A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C317/00Sulfones; Sulfoxides

Abstract

Pure aryl alkyl sulphones are made by subjecting substantially equimolar amounts of aluminium chloride and alkane sulphonyl chloride and an excess of an aromatic hydrocarbon or halogenated aromatic hydrocarbons to a Friedel-Crafts, reaction at a temperature substantially in the range 70-80 DEG C., for 7 to 12 hours, recovering the excess of the aromatic reactant and separating the aryl alkyl sulphone. The excess aromatic reactant may be recovered by distillation under reduced pressure and the sulphone isolated by cooling the reaction mixture, pouring the mixture on to ice and hydrochloric acid, extracting the sulphone with ether and distilling the solution, preferably at a pressure at or below 0.1 mm. mercury. Examples describe the preparation of p-fluorophenyl ethyl sulphone, p-fluorophenyl methyl sulphone and p-chlorophenyl ethyl sulphone.
GB3372862A 1961-09-14 1962-09-03 Improvements relating to the production of aryl alkyl sulphones Expired GB1010491A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR872194 1961-09-14

Publications (1)

Publication Number Publication Date
GB1010491A true GB1010491A (en) 1965-11-17

Family

ID=8762150

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3372862A Expired GB1010491A (en) 1961-09-14 1962-09-03 Improvements relating to the production of aryl alkyl sulphones

Country Status (1)

Country Link
GB (1) GB1010491A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1993018000A1 (en) * 1992-03-03 1993-09-16 Zeneca Limited Regioselective sulphonylation of substituted aromatic compounds

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1993018000A1 (en) * 1992-03-03 1993-09-16 Zeneca Limited Regioselective sulphonylation of substituted aromatic compounds
US5468903A (en) * 1992-03-03 1995-11-21 Zeneca Limited Regioselective sulfonylation reaction of substituted aromatic compounds

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