GB564412A - Preparation of thiazyl derivatives - Google Patents

Preparation of thiazyl derivatives

Info

Publication number
GB564412A
GB564412A GB10486/42A GB1048642A GB564412A GB 564412 A GB564412 A GB 564412A GB 10486/42 A GB10486/42 A GB 10486/42A GB 1048642 A GB1048642 A GB 1048642A GB 564412 A GB564412 A GB 564412A
Authority
GB
United Kingdom
Prior art keywords
mercapto
methyl
sodium
cyanoethyl
converted
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
GB10486/42A
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.)
Wingfoot Corp
Original Assignee
Wingfoot Corp
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 Wingfoot Corp filed Critical Wingfoot Corp
Publication of GB564412A publication Critical patent/GB564412A/en
Expired legal-status Critical Current

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  • Thiazole And Isothizaole Compounds (AREA)

Abstract

Cyanoethyl thiazyl sulphides and amides and esters thereof are prepared by combining 2-mercaptothiazoles with acrylonitrile in presence of an alkali metal or alkaline compound thereof, such as sodium, sodium hydroxide, sodium alcoholates, sodium mercaptides, or potassium hydroxide or a basic tertiary amine as catalyst. 2 - Mercaptobenzothiazole, 2-mercapto - 4 - methylthiazole, 2 - mercapto - 4 - phenyl thiazole, or any 2-mercapto naphthol thiazole or any 2-mercapto benzothiazole, such as 2-mercapto-5-methyl-, 2-mercapto-6-methyl-, 2 - mercapto - 4,6 - dimethyl-, 2 - mercapto - 4 - methyl-, 2 - mercapto - 4 - methyl - 6 - chlor-, 2-mercapto-6-ethoxy-, 2-mercapto-6-nitro-, and 2 - mercapto - 6 - amino - benzothiazole may be used. An example is given of the preparation of b -cyanoethyl benzothiazyl sulphide. The nitriles may be converted to amides by acid hydrolysis, e.g. b -(2-thiobenzothiazyl) propionamide which may be converted to the acid, e.g. carboxyethyl benzothiazyl sulphide, which may be converted to the ethyl or other alkyl, allyl, furyl or aryl ester. The esters may also be prepared by alcoholysis of cyanoethyl benzothiazyl sulphide in presence of gaseous HCl.
GB10486/42A 1942-04-25 1942-07-27 Preparation of thiazyl derivatives Expired GB564412A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US564412XA 1942-04-25 1942-04-25

Publications (1)

Publication Number Publication Date
GB564412A true GB564412A (en) 1944-09-27

Family

ID=22004423

Family Applications (1)

Application Number Title Priority Date Filing Date
GB10486/42A Expired GB564412A (en) 1942-04-25 1942-07-27 Preparation of thiazyl derivatives

Country Status (1)

Country Link
GB (1) GB564412A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4696763A (en) * 1984-05-11 1987-09-29 Ciba-Geigy Corporation Compositions containing heterocyclic corrosion inhibitors
US4719036A (en) * 1984-05-11 1988-01-12 Ciba-Geigy Corporation Compositions containing heterocyclic corrosion inhibitors

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4696763A (en) * 1984-05-11 1987-09-29 Ciba-Geigy Corporation Compositions containing heterocyclic corrosion inhibitors
US4719036A (en) * 1984-05-11 1988-01-12 Ciba-Geigy Corporation Compositions containing heterocyclic corrosion inhibitors

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