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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 479265생성일: 2026년 10월 24일

Dichloromethane → Triphenylsulfonium perfluorooctanesulfonate

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

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참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물Triphenylsulfonium BromideHCID 11984010—
반응물Potassium perfluorooctanesulfonateHCID 23669238—
용매WaterHCID 962—
생성물Triphenylsulfonium perfluorooctanesulfonateHCID 21863781—

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온도50 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06645698B1
출처 데이터셋uspto-grants-2003_11
ORD IDord-33260386189244328ed78539ca8fe351
출처 메모uspto-grants-2003_11