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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1702849생성일: 2026년 10월 23일

Hexafluoropropylene → 1,2-Oxathietane, 3,4,4-trifluoro-3-(trifluoromethyl)-, 2,2-dioxide

https://huagongshe.com/ko/reaction/1702849

반응식

참여 물질

역할이름HCID투입량
반응물HexafluoropropyleneHCID 8302—
반응물Sulfur trioxideHCID 24682—
생성물1,2-Oxathietane, 3,4,4-trifluoro-3-(trifluoromethyl)-, 2,2-dioxideHCID 2776240—

반응 단계

A mixture of commercial liquid sulfur trioxide (10 ml) and hexafluoropropene (45 g, 0.30 mol) was sealed in a Carius tube at liquid nitrogen temperature, mixed well at 25° C., allowed to stand for 4 days at 25° C., and finally heated in a steam bath for 6 hours. From two such tubes, there was obtained by distillation, 3-(trifluoromethyl)-3,4,4-trifluoro-1-oxa-2-thiacyclobutane 2,2-dioxide (2-hydroxy-1-trifluoromethyl-1,2,2-trifluoroethane sulfonic acid sultone, D. C. England, M. A. Dietrich and R. V. Lindsey, Jr., J. Amer. Chem. Soc., 82, 6181 (1960)) (25 g, 22%) bp 44° C., and pentafluoro-2-propenyl fluorosulfate (hereinafter referred to as perfluoroallyl fluorosulfate) (73 g, 63%), bp 58°-60° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04349650
출처 데이터셋uspto-grants-1982_09
ORD IDord-5e2d8884d96b4b4eb643f6693d6ebd04
출처 메모uspto-grants-1982_09