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