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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 278159생성일: 2026년 10월 26일

Benzoyl Peroxide → 4-Cyano-3-fluorobenzyl bromide

https://huagongshe.com/reaction/278159

반응식

참여 물질

역할이름HCID투입량
반응물Benzoyl PeroxideHCID 7187—
반응물N-bromobutanimideHCID 67184—
반응물2-Fluoro-4-methylbenzonitrileHCID 2778443—
용매Carbon TetrachlorideHCID 5943—
생성물4-Cyano-3-fluorobenzyl bromideHCID 2778466—

반응 단계

To a solution of the product from Step C (22.2 g, 165 mmol) in 220 mL of carbontetrachloride was added N-bromosuccinimide (29.2 g, 164 mmol) and benzoylperoxide (1.1 g). The reaction was heated to reflux for 30 minutes, then cooled to room temperature. The solution was concentrated in vacuo to one-third the original volume, poured into EtOAc, washed with water, sat. aq. NaHCO3, and brine, then dried (Na2SO4), filtered, and concentrated in vacuo to provide the crude product. Analysis by 1H NMR indicated only partial conversion, so the crude material was resubjected to the same reaction conditions for 2.5 hours, using 18 g (102 mmol) of N-bromosuccinimide. After workup, the crude material was purified by silica gel chromatography (0-10% EtOAc/hexane) to provide the desired product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06358985B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-0820a53ea7a745d798d5c82f7b972f94
출처 메모uspto-grants-2002_03