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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2914Generated: October 26, 2026

Dichloromethane → Triphenylsulfonium 4-trifluoromethylbenzenesulfonate

https://huagongshe.com/reaction/2914

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantSodium CarbonateHCID 10340—
ReactantTriphenylsulfonium chlorideHCID 61343—
Reactant4-(Trifluoromethyl)benzenesulfonyl chlorideHCID 2777399—
SolventWaterHCID 962—
ProductTriphenylsulfonium 4-trifluoromethylbenzenesulfonateHCID 22057398—

Reaction Steps

A suspension of 4-trifluoromethylbenzenesulfonyl chloride (20.53 g, 83.9 mmol) in water (150 ml) containing sodium carbonate (9.43 g, 88.10 mmol) was heated at reflux for 22 hours. After cooling to room temperature, triphenylsulfonium chloride (50% aqueous solution, 50.00 g) was added over 15 minutes. After stirring the biphasic mixture for 30 minutes, dichloromethane (300 ml) was added and the mixture stirred at room temperature for 20 hours. The layers were separated and the organic layer washed with water (7×150 ml) until the washings were neutral (pH 7 ). After drying (MgSO4 ), removal of the solvent in vacuo gave a pale yellow foam which was further dried by heating at 80°-100° C. for 108 hours under vacuum. In this way, triphenylsulfonium 4 -trifluoromethylbenzenesulfonate was isolated as a pale yellow glass (36.77 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05731364
Source datasetuspto-grants-1998_03
ORD IDord-36355329f50b4fba91d75f1d3bd8c47f
Source noteuspto-grants-1998_03