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HRID 1636833作成日:2026年10月26日

Dichloromethane → Triphenylsulfonium perfluorooctanesulfonate

https://huagongshe.com/reaction/1636833

反応式

関与物質

役割名称HCID仕込み量
反応物DichloromethaneHCID 6344—
反応物Triphenylsulfonium BromideHCID 11984010—
反応物Potassium perfluorooctanesulfonateHCID 23669238—
溶媒WaterHCID 962—
生成物Triphenylsulfonium perfluorooctanesulfonateHCID 21863781—

反応条件

温度50 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06037107
出典データセットuspto-grants-2000_03
ORD IDord-9caaa60e2cae44c0a9a73bde6e9a5cdb
出典メモuspto-grants-2000_03