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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 584038Generated: October 26, 2026

Hexane → Sulfonium, triphenyl-, 1,1,1-trifluoromethanesulfonate (1:1)

https://huagongshe.com/reaction/584038

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantDiphenyl sulfoxideHCID 13679—
ReactantTrifluoromethanesulfonic acidHCID 62406—
SolventBenzeneHCID 241—
ProductSulfonium, triphenyl-, 1,1,1-trifluoromethanesulfonate (1:1)HCID 1172932092%

Reaction Steps

In 200 ml of benzene were dissolved 21.1 g (0.1 mol) of diphenylsulfoxide, and 42.0 g (0.2 mol) of trifluoroacetic acid anhydride were added dropwise thereto at 0 to 5° C., followed by stirring and stirred at 0 to 5° C. for 30 minutes. And then, 15.0 g (0.1 mol) of trifluoromethane sulfonic acid were added dropwise thereto at 0 to 5° C. and allowed to react with stirring at 0 to 20° C. for 3 hours. After completion of the reaction, 500 ml of n-hexane was poured into the resultant and the obtained oily substance separated by decantation was crystallized from methylene chloride/n-hexane, followed by filtration and drying, to give 37.9 g (yield: 92%) of triphenylsulfonium trifluoromethanesulfonate as a white crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06924323B2
Source datasetuspto-grants-2005_08
ORD IDord-76ad00ee7d6644eead5077931a8520a5
Source noteuspto-grants-2005_08