GB839417A - A process for the production of benzthiazole-2-dicycloalkyl-sulphenamides - Google Patents

A process for the production of benzthiazole-2-dicycloalkyl-sulphenamides

Info

Publication number
GB839417A
GB839417A GB2588258A GB2588258A GB839417A GB 839417 A GB839417 A GB 839417A GB 2588258 A GB2588258 A GB 2588258A GB 2588258 A GB2588258 A GB 2588258A GB 839417 A GB839417 A GB 839417A
Authority
GB
United Kingdom
Prior art keywords
dicycloalkyl
alkali metal
sulphenamides
benzthiazole
mercaptobenzthiazole
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
GB2588258A
Inventor
Friedrich Lober
Helmut Freytag
Ernst Kracht
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.)
Bayer AG
Original Assignee
Bayer 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 Bayer AG filed Critical Bayer AG
Priority to GB2588258A priority Critical patent/GB839417A/en
Publication of GB839417A publication Critical patent/GB839417A/en
Expired legal-status Critical Current

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  • Thiazole And Isothizaole Compounds (AREA)

Abstract

Benzthiazole - 2 - dicycloalkyl sulphenamides are prepared by reacting an N-dicycloalkyl amine, in which the cycloalkyl radicals may be substituted or unsubstituted and contain 5 to 7 ring carbon atoms, with an aqueous alkali metal hypochlorite solution to form the corresponding N - chloro - dicycloalkyl amine, and reacting this latter compound in the aqueous phase in the presence of a watersoluble aliphatic ketone (e.g. acetone, methyl ethyl ketone, methyl propyl ketone or diacetone alcohol) with an alkali metal or alkaline earth metal salt of 2-mercaptobenzthiazole. The second stage of the reaction may be carried out in presence of 0.05 to 0.25 mol. of an alkali metal hydroxide or alkaline earth metal hydroxide per mol. of mercaptobenzthiazole. Specifications 377,730, 713,496, 737,252 and 753,803 are referred to.
GB2588258A 1958-08-12 1958-08-12 A process for the production of benzthiazole-2-dicycloalkyl-sulphenamides Expired GB839417A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB2588258A GB839417A (en) 1958-08-12 1958-08-12 A process for the production of benzthiazole-2-dicycloalkyl-sulphenamides

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB2588258A GB839417A (en) 1958-08-12 1958-08-12 A process for the production of benzthiazole-2-dicycloalkyl-sulphenamides

Publications (1)

Publication Number Publication Date
GB839417A true GB839417A (en) 1960-06-29

Family

ID=10234907

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2588258A Expired GB839417A (en) 1958-08-12 1958-08-12 A process for the production of benzthiazole-2-dicycloalkyl-sulphenamides

Country Status (1)

Country Link
GB (1) GB839417A (en)

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