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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 479265Erstellt: 24. Oktober 2026

Dichloromethane → Triphenylsulfonium perfluorooctanesulfonate

https://huagongshe.com/de/reaction/479265

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDichloromethaneHCID 6344—
EduktTriphenylsulfonium BromideHCID 11984010—
EduktPotassium perfluorooctanesulfonateHCID 23669238—
LösungsmittelWaterHCID 962—
ProduktTriphenylsulfonium perfluorooctanesulfonateHCID 21863781—

Reaktionsbedingungen

Temperatur50 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06645698B1
Quelldatensatzuspto-grants-2003_11
ORD IDord-33260386189244328ed78539ca8fe351
Quellennotizuspto-grants-2003_11