GB895701A - Process for the manufacture of thiophenemono-sulphochlorides - Google Patents
Process for the manufacture of thiophenemono-sulphochloridesInfo
- Publication number
- GB895701A GB895701A GB35894/59A GB3589459A GB895701A GB 895701 A GB895701 A GB 895701A GB 35894/59 A GB35894/59 A GB 35894/59A GB 3589459 A GB3589459 A GB 3589459A GB 895701 A GB895701 A GB 895701A
- Authority
- GB
- United Kingdom
- Prior art keywords
- thiophene
- sulphochlorides
- reacted
- reacting
- prepared
- 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
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D333/30—Hetero atoms other than halogen
- C07D333/34—Sulfur atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
Abstract
Chlorosulphonic acid and phosphorus pentachloride are reacted in a molar ratio of from 2 : 1 to 3 : 1 at - 20 DEG C. to +20 DEG C.; HCl is evolved. The product (not identified) is a mild sulphochlorination agent (see Group IV(b)).ALSO:Thiophene sulphochlorides of formula <FORM:0895701/IV (b)/1> where R is hydrogen, halogen (e.g. chloro, bromo and iodo), or an alkyl group having 1-6 carbon atoms, are prepared by reacting the 2-R-thiophene with a mixture of chlorsulphonic acid and phosphorus pentachloride or with a reaction product of these two compounds. Thus chlorsulphonic acid and PCl5 may be reacted at -20 DEG C. to +20 DEG C., the thiophene added, and the mixture heated at 20 DEG C.-70 DEG C. 2-Chlorothiophene-5-sulphonamide is prepared by reacting the sulphochloride with ammonia.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE895701X | 1958-10-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB895701A true GB895701A (en) | 1962-05-09 |
Family
ID=6847821
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB35894/59A Expired GB895701A (en) | 1958-10-22 | 1959-10-22 | Process for the manufacture of thiophenemono-sulphochlorides |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB895701A (en) |
-
1959
- 1959-10-22 GB GB35894/59A patent/GB895701A/en not_active Expired
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