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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1003922Generated: October 25, 2026

Dichloromethane → Triphenylsulfonium perfluorooctanesulfonate

https://huagongshe.com/reaction/1003922

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTriphenylsulfonium BromideHCID 11984010—
ReactantPotassium perfluorooctanesulfonateHCID 23669238—
SolventWaterHCID 962—
ProductTriphenylsulfonium perfluorooctanesulfonateHCID 21863781—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a suspension of perfluorooctanesulfonic acid potassium salt (10.76 g, 20.0 mmol) in water (100 mL) at room temperature under nitrogen was added dropwise triphenylsulfonium bromide (6.87 g, 20.0 mmol) over 15 min. After stirring the suspension for 30 min., dichloromethane (100 mL) was added and the biphasic mixture stirred at room temperature for 20 h. Additional dichloromethane (100 mL) was added and the layers separated. The organic layer was washed with water (3×75 mL) until the washings were neutral (pH 7). After drying (MgSO4), removal of the solvent in vacuum gave a viscous gum which was further dried by heating at 50° C. for 24 h under vacuum. In this way, triphenylsulfonium perfluorooctanesulfonate was isolated as a pale yellow gummy solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06048672
Source datasetuspto-grants-2000_04
ORD IDord-ec5edefbec254454b7cf45af3647c17f
Source noteuspto-grants-2000_04