GB897735A - Improvements in or relating to methods of producing aromatic sulphones - Google Patents
Improvements in or relating to methods of producing aromatic sulphonesInfo
- Publication number
- GB897735A GB897735A GB2552658A GB2552658A GB897735A GB 897735 A GB897735 A GB 897735A GB 2552658 A GB2552658 A GB 2552658A GB 2552658 A GB2552658 A GB 2552658A GB 897735 A GB897735 A GB 897735A
- Authority
- GB
- United Kingdom
- Prior art keywords
- reaction
- compound
- sulphohalide
- halogen atom
- formula
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C317/00—Sulfones; Sulfoxides
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
A method of producing aromatic sulphones comprises reacting a compound of the formula RH with a sulphohalide of the formula R1SO2X where R represents a phenyl, naphthyl or thienyl residue substituted by at least one halogen atom or by at least one hydrocarbon radical or by at least one ether or thio-ether group or represents an unsubstituted thienyl residue, R1 represents a phenyl or naphthyl residue which may be substituted by at least one halogen atom, at least one hydrocarbon radical or at least one ether or thio-ether group and X represents a halogen atom, the compound RH and the sulphohalide containing no free hydroxyl, sulph-hydryl or amino groups, the reaction being carried out in the presence of a metal (other than alkali or alkaline earth metal) salt of ortho-, meta or pyro-phosphoric acid or a mixture thereof, so that sulphones of the formula RSO2R1 are produced. The reaction is preferably carried out by slowly adding the metal salt and/or sulphohalide to the compound RH at a temperature of 100 DEG C.-150 DEG C. and a diluent such as a nitro-alkene or an excess of the compound RH may be used. The reaction is preferably carried out under anhydrous conditions but to enable the reaction to proceed to completion a trace of water may be added to the reactants. In the examples in which silver, zinc and cadmium salts are used, 4-methoxy-, 4,41-dimethoxy-, 4-methyl, 4-methoxy-41 - chloro - and 2,4,5,41 - tetrachloro - diphenyl sulphone and 4-methoxyphenyl thienyl sulphone are prepared. Specification 761,837 is referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL219871 | 1957-08-13 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB897735A true GB897735A (en) | 1962-05-30 |
Family
ID=19750949
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2552658A Expired GB897735A (en) | 1957-08-13 | 1958-08-08 | Improvements in or relating to methods of producing aromatic sulphones |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB897735A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1993018000A1 (en) * | 1992-03-03 | 1993-09-16 | Zeneca Limited | Regioselective sulphonylation of substituted aromatic compounds |
-
1958
- 1958-08-08 GB GB2552658A patent/GB897735A/en not_active Expired
Cited By (2)
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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