돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1447472생성일: 2026년 10월 26일

Fluorosulfuric acid → Difluoromalonyl fluoride

https://huagongshe.com/reaction/1447472

반응식

참여 물질

역할이름HCID투입량
반응물Fluorosulfuric acidHCID 24603—
반응물Methyl 2,2,3-trifluoro-3-oxopropanoateHCID 93396—
생성물Difluoromalonyl fluorideHCID 277409965%

반응 단계

A mixture of 624 g (4.0 mol) of methyl difluorofluoroformylacetate, 348 g (3.5 mol) of fluorosulfonic acid and 25 ml of HSbF6 (0.3 mol) was charged to a 1 liter Teflon® pot fitted with a Teflon® condenser connected to a trap cooled to -80°. The mixture was stirred and heated at 80° to 110° for about 24 h. Then, 187 g (65% yield) of crude difluoromalonyl fluoride was collected which, after trap-to-trap distillation, was analyzed by NMR at -30°. NMR (CCl4): 19F 21.0 (t, JFF 10.9 Hz, 2F, COF) and -112.4 ppm (t, JFF 10.9 Hz, 2F, CF2) with a very small amount of impurity showing at -162.1 ppm. Distillation of a 140 g sample gave 118 g of pure FCOCF2COF, b.p. -4° to -5°. Dimethyl difluoromalonate was also formed.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04316986
출처 데이터셋uspto-grants-1982_02
ORD IDord-e06c4b4a741e424c8372b32805392475
출처 메모uspto-grants-1982_02