GB387738A - Process of manufacturing 2-mercaptoarylthiazoles - Google Patents

Process of manufacturing 2-mercaptoarylthiazoles

Info

Publication number
GB387738A
GB387738A GB24884/31A GB2488431A GB387738A GB 387738 A GB387738 A GB 387738A GB 24884/31 A GB24884/31 A GB 24884/31A GB 2488431 A GB2488431 A GB 2488431A GB 387738 A GB387738 A GB 387738A
Authority
GB
United Kingdom
Prior art keywords
excess
sulphur
aniline
thiazole
product
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
GB24884/31A
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.)
Uniroyal Chemical Co Inc
Original Assignee
Naugatuck Chemical Co
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 Naugatuck Chemical Co filed Critical Naugatuck Chemical Co
Publication of GB387738A publication Critical patent/GB387738A/en
Expired legal-status Critical Current

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Abstract

A 2-mercaptoarylthiazole compound is prepared by reacting substantially two mols. of a primary arylamine with substantially three atoms of sulphur and then heating at a temperature less than 200 DEG C. under pressures of 100-500 pounds/sq. ins., the product with carbon disulphide in excess of theoretical requirements, and separating the thiazole formed. In the examples aniline and sulphur in the specified proportion are reacted together at 180 DEG C. and the product, after removing excess aniline, is heated in an autoclave at 150-160 DEG C. and 400 pounds/sq.-ins. pressure with excess carbon disulphide; the 2-mercaptobenzthiazole is extracted by solution in caustic soda followed by acidification with sulphuric acid. It is stated that aniline disulphide is formed in the first reaction and that the subsequent formation of side-products is diminished and of thiazole is increased by working as specified. The production of 2-mercaptotolyland xylyl-thiazoles in a similar manner is also mentioned. The Specification as open to inspection under Sect. 91 relates to the production of a 2-mercaptoarylthiazole by reacting a primary arylamine with sulphur, and then heating the reaction product, preferably under pressure, with carbon disulphide in excess of theoretical requirements, and separating the thiazole compound formed. This subject-matter does not appear in the Specification as accepted.
GB24884/31A 1930-09-22 1931-09-04 Process of manufacturing 2-mercaptoarylthiazoles Expired GB387738A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US387738XA 1930-09-22 1930-09-22

Publications (1)

Publication Number Publication Date
GB387738A true GB387738A (en) 1933-02-16

Family

ID=21901817

Family Applications (1)

Application Number Title Priority Date Filing Date
GB24884/31A Expired GB387738A (en) 1930-09-22 1931-09-04 Process of manufacturing 2-mercaptoarylthiazoles

Country Status (1)

Country Link
GB (1) GB387738A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4028473A1 (en) * 1990-09-07 1992-03-12 Akzo Gmbh METHOD FOR PRODUCING 2-MERCAPTO-BENZOTHIAZOL
US5367082A (en) * 1990-09-07 1994-11-22 Akzo N.V. Process for the preparation of 2-mercaptobenzothiazole

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4028473A1 (en) * 1990-09-07 1992-03-12 Akzo Gmbh METHOD FOR PRODUCING 2-MERCAPTO-BENZOTHIAZOL
US5367082A (en) * 1990-09-07 1994-11-22 Akzo N.V. Process for the preparation of 2-mercaptobenzothiazole

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