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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1920612Generated: November 2, 2026

Hydrochloric Acid → 4-Fluorophenyldiphenylsulfonium chloride

https://huagongshe.com/reaction/1920612

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantBenzene, 1-chloro-4-fluoro-HCID 9604—
ReactantDiphenyl sulfoxideHCID 13679—
ReactantMagnesiumHCID 5462224—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product4-Fluorophenyldiphenylsulfonium chlorideHCID 86649660—

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, 78.3 g (0.6 mole) of 4-fluorochlorobenzene and 180 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 4-fluorophenyldiphenylsulfonium 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 numberUS08173354B2
Source datasetuspto-grants-2012_05
ORD IDord-9e58f05476904428a99705af8f21d670
Source noteuspto-grants-2012_05