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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1257163생성일: 2026년 10월 25일

Methanesulfonyl chloride → 3-Acetamido-6-chloro-2-fluorobenzyl methanesulfonate

https://huagongshe.com/reaction/1257163

반응식

참여 물질

역할이름HCID투입량
반응물Methanesulfonyl chlorideHCID 31297—
반응물N-(4-chloro-2-fluoro-3-(hydroxymethyl)phenyl)acetamideHCID 86713625—
용매DichloromethaneHCID 6344—
생성물3-Acetamido-6-chloro-2-fluorobenzyl methanesulfonateHCID 8671362691.9%

반응 단계

A 0° C. of N-(4-chloro-2-fluoro-3-(hydroxymethyl)phenyl)acetamide (1.05 g, 4.82 mmol) and TEA (1.003 mL, 7.24 mmol) in DCM (30 mL) was treated slowly with methanesulfonyl chloride (0.414 mL, 5.31 mmol), warmed to RT and stirred for 2 h. The mixture was treated with satd. NaHCO3, extracted with DCM (2×) and the combined organics were washed with brine, dried over Na2SO4 and concentrated to dryness to afford 3-acetamido-6-chloro-2-fluorobenzyl methanesulfonate (1.31 g, 74% yield) as an off-white solid. MS (ESI) m/z: 296.0 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08461179B1
출처 데이터셋uspto-grants-2013_06
ORD IDord-b6cd181252794d948d2e9d900a4deed8
출처 메모uspto-grants-2013_06