Sulfene - Preparation

Preparation

The first general method for preparation of sulfene as an intermediate, reported simultaneously in 1962 by Gilbert Stork and by Günther Optiz, involved removal of hydrogen chloride from methanesulfonyl chloride using triethylamine in the presence of an enamine as trapping agent. The formation of a thietane 1,1-dioxide derivative was taken as evidence for the intermediacy of sulfene. Because of the highly electrophilic character of sulfene, the use of amines presents difficulties, since they can intercept the sulfene to form complexes, which may display reduced activity in trapping reactions compared to sulfene itself. A simple alternative which avoids the use of amines involves desilylation of trimethylsilylmethanesulfonyl chloride with cesium fluoride in the presence of trapping agents.

(CH3)3SiCH2SO2Cl + CsF → + (CH3)3SiF + CsCl

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