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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 3952생성일: 2026년 10월 23일

Tetrahydrofuran → Potassium 1,1,2,2-tetrafluoro-2-(pentafluoroethoxy)ethane-1-sulfonate

https://huagongshe.com/ko/reaction/3952

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물1,1,2,2-tetrafluoro-2-(1,1,2,2,2-pentafluoroethoxy)ethanesulfonyl FluorideHCID 2782567—
반응물Potassium trimethylsilanolateHCID 23668039—
용매GlycerolHCID 753—
생성물Potassium 1,1,2,2-tetrafluoro-2-(pentafluoroethoxy)ethane-1-sulfonateHCID 278241565%

반응 단계

The procedure of Example 1 was followed using perfluoro-3-oxapentanesulfonyl fluoride (7.95 g, 25 mmol), potassium trimethylsilanolate (3.2 g, 25 mmol) and dry tetrahydrofuran (100 mL) while heating at reflux for 1.5 h. Potassium perfluoro-3-oxapentanesulfonate (3.79 g initially and 1.74 g by concentrating the filtrate under vacuum; total 5.53 g, 65% yield) was isolated as a white solid: 19F NMR (fluorotrichloromethane) δ -79.4 (m, CF2, 2F), -83.2 (s, CF3, 3F), -84.9 (m, CF2, 2F), -115.0 ppm (m, CF2, 2F); Positive ion Fast Atom Bombardment MS (Glycerol matrix, Cs⊕ ion bombardment) m/e 393, 747, 1101, 1455, 1809 for M+K⊕ to M5 +K⊕.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04723016
출처 데이터셋uspto-grants-1988_02
ORD IDord-bced94d3b141486e89edeb33840b194b
출처 메모uspto-grants-1988_02