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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212624Generated: November 2, 2026

Diphenylmethane → HCID 21964751, compound

https://huagongshe.com/reaction/2212624

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiphenylmethaneHCID 7580—
ReactantTrifluoroacetic anhydrideHCID 9845—
ReactantDiphenyl sulfoxideHCID 13679—
ReactantTrifluoromethanesulfonic acidHCID 62406—
SolventWaterHCID 962—
SolventHexaneHCID 8058—
ProductHCID 21964751HCID 2196475175%

Reaction Steps

In 35 ml of n-hexane were suspended 6.07 g (0.03 mol) of diphenylsulfoxide and 6.06 g (0.036 mol) of diphenylmethane, and 7.56 g (0.036 mol) of trifluoroacetic anhydride was added thereto at 0° C. Then 4.5 g (0.03 mol) of trifluoromethanesulfonic acid was added dropwise thereto at 0 to 5° C., followed by gradually warming to room temperature and reacting for 4 hours with stirring. After completion of the reaction, 50 ml of water was poured into the reaction solution and the n-hexane layer was removed by fractionation. The aqueous layer was further washed with 50 ml of hexane three times and extracted with 60 ml of dichloromethane. The resulting dichloromethane layer was washed with 50 ml of water five times, followed by concentration under reduced pressure. 70 ml of ethyl acetate was poured into the resulting crude crystal, followed by dissolving by warming to 60° C., cooling to room temperature, the resulting crude crystal was filtered and dried under vacuum to obtain 11.3 g (Yield: 75%) of diphenyl-4-phenylmethylphenylsulfonium trifluoromethanesulfonate as a pale brown crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07101918B2
Source datasetuspto-grants-2006_09
ORD IDord-8959bfd50d794ea18d3cb0a01f028bce
Source noteuspto-grants-2006_09