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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 424326Generated: October 30, 2026

Hydrochloric Acid → Triphenylsulfonium chloride

https://huagongshe.com/reaction/424326

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantChlorobenzeneHCID 7964—
ReactantDiphenyl sulfoxideHCID 13679—
ReactantMagnesiumHCID 5462224—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductTriphenylsulfonium chlorideHCID 61343—

Reaction Steps

Diphenyl sulfoxide, 40 g (0.2 mole), was dissolved in 400 g of dichloromethane, which was stirred under ice cooling. At a temperature below 20° C., 65 g (0.6 mole) of trimethylsilyl chloride was added dropwise to the solution, which was allowed to mature for 30 minutes at the temperature. Then, a Grignard reagent which had been prepared from 14.6 g (0.6 mole) of metallic magnesium, 67.5 g (0.6 mole) of chlorobenzene and 168 g of tetrahydrofuran (THF) was added dropwise at a temperature below 20° C. The reaction solution was allowed to mature for one hour, after which 50 g of water at a temperature below 20° C. was added to quench the reaction. To this solution, 150 g of water, 10 g of 12N hydrochloric acid, and 200 g of diethyl ether were further added. The water layer was separated and washed with 100 g of diethyl ether, yielding an aqueous solution of triphenylsulfonium chloride. The compound in aqueous solution form was used in the subsequent reaction without further isolation.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08105748B2
Source datasetuspto-grants-2012_01
ORD IDord-3bb217eaff084bca82649e2ccc5ab6fe
Source noteuspto-grants-2012_01