GB398947A - The manufacture of arylisothiazolones - Google Patents

The manufacture of arylisothiazolones

Info

Publication number
GB398947A
GB398947A GB1275732A GB1275732A GB398947A GB 398947 A GB398947 A GB 398947A GB 1275732 A GB1275732 A GB 1275732A GB 1275732 A GB1275732 A GB 1275732A GB 398947 A GB398947 A GB 398947A
Authority
GB
United Kingdom
Prior art keywords
sulphochloride
benzene
ethoxy
cyano
acid
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
GB1275732A
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.)
IG Farbenindustrie AG
Original Assignee
IG Farbenindustrie AG
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 IG Farbenindustrie AG filed Critical IG Farbenindustrie AG
Priority to GB1275732A priority Critical patent/GB398947A/en
Publication of GB398947A publication Critical patent/GB398947A/en
Expired legal-status Critical Current

Links

Abstract

Arylisothiazolones are obtained by treating aryl - o - cyanosulphochlorides with metallic reducing agents in presence of a mineral acid and an organic solvent at temperatures below 60 DEG . The amount of reducing agent is such as to liberate four reactive hydrogen atoms per molecule of sulphochloride and the reaction is taken to such a point that a test fails to show the mercaptan reaction. According to examples, 1 - methyl - 2-cyan - 5-chlor-benzene-3-sulphonic acid after conversion to the sulphochloride with phosphorus pentachloride gives 4-methyl-6-chloro-benz-isothiazolone-3, and 1-ethoxy-4-amino-benzene - 5 - sulphochloride (obtained by converting 1 - ethoxy - 4 - amino-benzene-5-sulphonic acid into the 4-cyano compound and treating with phosphorus pentachloride) gives 6 - ethoxy-benz-isothiazolone - 3, on treatment with zinc dust and hydrochloric or sulphuric acid respectively. Cyano-benzene-o-sulphochloride and naphthalene-2-cyano-1-sulphochloride are also specified and glacial acetic acid and other metallic reducing agents such as tin may be employed. British Specification 319,075, [Class 2 (iii), Dyes &c.], and German Specification 216,269 are referred to.
GB1275732A 1932-05-03 1932-05-03 The manufacture of arylisothiazolones Expired GB398947A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1275732A GB398947A (en) 1932-05-03 1932-05-03 The manufacture of arylisothiazolones

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1275732A GB398947A (en) 1932-05-03 1932-05-03 The manufacture of arylisothiazolones

Publications (1)

Publication Number Publication Date
GB398947A true GB398947A (en) 1933-09-28

Family

ID=10010559

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1275732A Expired GB398947A (en) 1932-05-03 1932-05-03 The manufacture of arylisothiazolones

Country Status (1)

Country Link
GB (1) GB398947A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3065123A (en) * 1959-06-24 1962-11-20 Ici Ltd Process for control of micro-organisms

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3065123A (en) * 1959-06-24 1962-11-20 Ici Ltd Process for control of micro-organisms

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