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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1703생성일: 2026년 10월 23일

Carbon Dioxide → 2,2,2-Trifluoroethyl trifluoromethanesulfonate

https://huagongshe.com/ko/reaction/1703

반응식

참여 물질

역할이름HCID투입량
반응물Carbon DioxideHCID 280—
반응물2,2,2-TrifluoroethanolHCID 6409—
반응물TriethylamineHCID 8471—
반응물Trifluoromethanesulfonyl chlorideHCID 79000—
용매Diethyl EtherHCID 3283—
용매IsopropanolHCID 3776—
용매DichloromethaneHCID 6344—
생성물2,2,2-Trifluoroethyl trifluoromethanesulfonateHCID 80366—

반응 조건

온도0 °C

반응 단계

A solution of trifluoromethanesulfonyl chloride (800 uL, 7.5 mmole) in CH2Cl2 (6 mL) was cooled under argon to -60° C. (IPA:dry ice bath). 2,2,2-Trifluoroethanol was added (456 uL, 6 mmol) and triethylamine (1.04 uL, 7.5 mmol) was added dropwise. The reaction was stirred for 1.5 hours then warmed to 0° C. for 1 hour. Anhydrous ether (20 mL) was added and the mixture was stirred at 0° C. for 30 minutes. The solids were filtered off and the solvent was removed under reduced pressure with the flask maintained at 0° C. This afforded the 2,2,2-trifluoroethyltriflate as a yellow oil which was used immediately.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05726172
출처 데이터셋uspto-grants-1998_03
ORD IDord-c1eb50330c204669ac80b93517bb8dec
출처 메모uspto-grants-1998_03