GB497659A - Manufacture of 2-alkyl-tetrahydrobenzselenazoles - Google Patents

Manufacture of 2-alkyl-tetrahydrobenzselenazoles

Info

Publication number
GB497659A
GB497659A GB17351/37A GB1735137A GB497659A GB 497659 A GB497659 A GB 497659A GB 17351/37 A GB17351/37 A GB 17351/37A GB 1735137 A GB1735137 A GB 1735137A GB 497659 A GB497659 A GB 497659A
Authority
GB
United Kingdom
Prior art keywords
cyclohexanone
alkyl
thio
seleno
chloro
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
GB17351/37A
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
Publication of GB497659A publication Critical patent/GB497659A/en
Expired legal-status Critical Current

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  • Thiazole And Isothizaole Compounds (AREA)

Abstract

2-Alkyl-tetrahydrobenzthiazoles and 2-alkyl-tetrahydrobenzselenazoles are prepared by causing an ortho-halogen-cyclohexanone to react with a thio-fatty acid amide or a seleno-fatty acid amide or a substituted thio- or seleno-fatty acid amide. The compounds have the general formula <FORM:0497659/IV/1> where Y=sulphur or selenium, and R=an alkyl or a substituted alkyl group. The reaction is preferably conducted at a raised temperature. In examples: (1) o-chloro-cyclohexanone and thio-acetamide are heated together, and the reaction product treated with caustic soda, and the oil so liberated extracted with ether. The residue on evaporation of the ether is distilled under reduced pressure to give 2-methyl-tetra-hydro - benzothiazole; (2) o - chloro - cyclohexanone, alcohol and seleno-acetamide are heated together, the reaction product is taken up in water and filtered from the precipitated selenium. Caustic soda is added to the filtrate to precipitate the 2-methyl-tetrahydro-benzselenazole; (3) o-chloro-cyclohexanone and thio-propionamide are heated together and the product treated with caustic soda to give 2-ethyl-tetrahydrobenzothiazole.
GB17351/37A 1936-07-29 1937-06-22 Manufacture of 2-alkyl-tetrahydrobenzselenazoles Expired GB497659A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE497659X 1936-07-29

Publications (1)

Publication Number Publication Date
GB497659A true GB497659A (en) 1938-12-22

Family

ID=6545208

Family Applications (1)

Application Number Title Priority Date Filing Date
GB17351/37A Expired GB497659A (en) 1936-07-29 1937-06-22 Manufacture of 2-alkyl-tetrahydrobenzselenazoles

Country Status (1)

Country Link
GB (1) GB497659A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4208420A (en) * 1977-10-24 1980-06-17 Laboratoires Jacques Logeais New benzo [d] thiazole derivatives, process for their preparation and their therapeutic applications

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4208420A (en) * 1977-10-24 1980-06-17 Laboratoires Jacques Logeais New benzo [d] thiazole derivatives, process for their preparation and their therapeutic applications

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