Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212625Generated: November 2, 2026

Diphenyl sulfide → HCID 21964992, compound

https://huagongshe.com/reaction/2212625

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiphenyl sulfideHCID 8766—
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantDiphenyl sulfoxideHCID 13679—
ReactantPerfluorobutanesulfonic acidHCID 67815—
SolventDichloromethaneHCID 6344—
ProductHCID 21964992HCID 2196499278%

Reaction Steps

In 50 ml of dichloromethane were dissolved 6.07 g (0.03 mol) of diphenylsulfoxide and 11.2 g (0.06 mol) of diphenylsulfide, and 7.56 g (0.036 mol) of trifluoroacetic anhydride was poured thereinto at 0° C. Then 9.0 g (0.03 mol) of nonafluorobutanesulfonic acid was added dropwise at 0 to 5° C., followed by gradually warming to room temperature and reacting for 2 hours with stirring. After completion of the reaction, the reaction solution was washed with 100 ml of water five times and concentrated under reduced pressure, followed by purifying the resulting crude product by a column chromatography to obtain 7.85 g (Yield: 39%) of diphenyl-4-phenylthiophenylsulfonium nonafluorobutanesulfonate as a yellow oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07101918B2
Source datasetuspto-grants-2006_09
ORD IDord-20fae3de48f14acf8c6fe0dd4b4e5d16
Source noteuspto-grants-2006_09