A NEW ROUTE TO THIOSULFONATE AND SELENOSULFONATE FROM DISULFIDES AND DISELENIDES - APPLICATION TO THE SYNTHESIS OF NEW THIOESTER AND SELENOESTER OF TRIFLIC ACID

Citation
T. Billard et al., A NEW ROUTE TO THIOSULFONATE AND SELENOSULFONATE FROM DISULFIDES AND DISELENIDES - APPLICATION TO THE SYNTHESIS OF NEW THIOESTER AND SELENOESTER OF TRIFLIC ACID, Journal of organic chemistry, 61(21), 1996, pp. 7545-7550
Citations number
68
Categorie Soggetti
Chemistry Inorganic & Nuclear
ISSN journal
00223263
Volume
61
Issue
21
Year of publication
1996
Pages
7545 - 7550
Database
ISI
SICI code
0022-3263(1996)61:21<7545:ANRTTA>2.0.ZU;2-J
Abstract
Alkyl and aryl trifluoromethanethiosulfonates(1) (or selenosulfonates) were prepared in one step either from alkyl and aryl sulfenyl (or sel enenyl) chlorides and sodium trifluoromethanesulfinate (3) or, more ge nerally, from disulfides (or diselenides), 3, and bromine. The second method involved trifluoromethanesulfonyl bromide as key intermediate. Benzenethiosulfonates were obtained in a similar way from disulfides, benzenesulfinate, and bromine but benzeneselenosulfonates could not be obtained by the same method from diselenides.