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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 19936생성일: 2026년 10월 23일

Water → 3-Benzoyloxy-4-fluorobenzyl bromide

https://huagongshe.com/ko/reaction/19936

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Benzoyl PeroxideHCID 7187—
반응물N-bromobutanimideHCID 67184—
반응물3-Benzoyloxy-4-fluorotolueneHCID 16749220—
용매Diethyl EtherHCID 3283—
용매Carbon TetrachlorideHCID 5943—
생성물3-Benzoyloxy-4-fluorobenzyl bromideHCID 16747838—

반응 단계

A mixture of benzoic acid 2-fluoro-5-methyl-phenyl ester (CAB02145, 2.47 g, 10.0 mmol), N-bromo-succinimide (1.96 g, 11.0 mmol) and dibenzoylperoxide (10 mg) in carbon tetrachloride (25 mL) was heated to reflux for 2 h (TLC monitored). After cooling to room temperature, water (50 mL) and diethyl ether (100 mL) were added. The organic layer was separated, washed with brine (20 mL), dried over sodium sulphate and concentrated under reduced pressure. The residue was purified by column chromatography (EtOAc:hexane, 1:25, Rf: 0.28). Yield: 1.80 g (58%), white solid. 1H-NMR (400 MHz, CDCl3) δ=4.48 (s, 2H, —CH2Br), 7.18 (dd, J=9.8, 8.6 Hz, 1H), 7.28 (ddd, J=8.6, 4.3, 2.3 Hz, 1H), 7.34 (dd, J=7.0, 2.3 Hz, 1H), 7.50-7.55 (m, 2H), 7.64-7.69 (m, 1H), 8.18-8.23 (m, 2H). LRMS (FAB+): 229.1 (95), 309.0 (100, [M+]+). Found: C, 54.1, H, 3.22%; C14H10BrFO2 (309.13) requires C, 54.39, H, 3.26%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745472B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-fcb20ac347e042dcb5f0de838d995e0f
출처 메모uspto-grants-2010_06