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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2913Generated: October 24, 2026

Dichloromethane → Triphenylsulfonium perfluorooctanesulfonate

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Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTriphenylsulfonium chlorideHCID 61343—
ReactantPotassium perfluorooctanesulfonateHCID 23669238—
SolventWaterHCID 962—
ProductTriphenylsulfonium perfluorooctanesulfonateHCID 21863781—

Reaction Steps

To a suspension of perfluorooctanesulfonic acid potassium salt (24.64 g, 46.1 mmol) in water (150 ml) at room temperature under nitrogen was added dropwise triphenylsulfonium chloride (50% aqueous solution, 27.50 g) over 15 minutes. After stirring the suspension for 30 minutes, dichloromethane (75 ml) was added and the mixture stirred at room temperature for 20 hours. Additional dichloromethane (225 ml) was added and the layers separated. The organic layer was washed with water (5×125 ml) until the washings were neutral (pH 7 ). After drying (MgSO4 ), removal of the solvent in vacuo gave a viscous gum which was further dried by heating at 80°-90° C. for 84 hours under vacuum. In this way, triphenylsulfonium perfluorooctanesulfonate was isolated as a glassy solid (30.61 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05731364
Source datasetuspto-grants-1998_03
ORD IDord-d1e6e90adf2744bfa6b435f6c7114ace
Source noteuspto-grants-1998_03