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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 17005생성일: 2026년 10월 23일

Sodium hydride → 2,2,2-Trifluoro-1-(4-fluorophenyl)ethyl trifluoromethanesulfonate

https://huagongshe.com/ko/reaction/17005

반응식

참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물Trifluoromethanesulfonyl chlorideHCID 79000—
반응물2,2,2-Trifluoro-1-(4-fluorophenyl)ethanolHCID 11148246—
용매Diethyl EtherHCID 3283—
용매HexaneHCID 8058—
생성물2,2,2-Trifluoro-1-(4-fluorophenyl)ethyl trifluoromethanesulfonateHCID 57562097101.2%

반응 단계

NaH (640 mg, 16 mmol, 60% in mineral oil) was washed twice with hexane (20 mL) and then suspended in dried diethyl ether (20 mL). A solution of 2,2,2-trifluoro-1-(4-fluoro-phenyl)ethanol (1.94 g, 10 mmol) in diethyl ether (10 mL) was added at 0° C. After stirring for 2 h at room temperature, a solution of trifluoromethanesulfonyl chloride (1.68 g, 10 mmol) in diethyl ether (10 mL) was added. After 2 h, the reaction mixture was quenched by adding a solution of NaHCO3 and the product was extracted with diethyl ether. The extracts were washed with brine and dried, and the solvent was removed to yield trifluoromethanesulfonic acid 2,2,2-trifluoro-1-(4-fluorophenyl)ethyl ester (3.3 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737300B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-28c59b0678af4521a6e78ceace972cf5
출처 메모uspto-grants-2010_06