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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 224289생성일: 2026년 10월 26일

Benzoyl Peroxide → Ethyl 2-bromo-2-(3,4-dichlorophenyl)acetate

https://huagongshe.com/reaction/224289

반응식

참여 물질

역할이름HCID투입량
반응물Benzoyl PeroxideHCID 7187—
반응물N-bromobutanimideHCID 67184—
반응물Ethyl 3,4-dichlorophenylacetateHCID 2737422—
용매Carbon TetrachlorideHCID 5943—
생성물Ethyl 2-bromo-2-(3,4-dichlorophenyl)acetateHCID 12717583—

반응 단계

In a three-necked flask fitted with a Nichrome stirrer and a reflux condenser is placed 7.0 g of ethyl 3,4-dichlorophenylacetate, 5.9 g of N-bromosuccinimide, 0.1 g of benzoyl peroxide and 150 ml of carbon tetrachloride. The reaction mixture is heated at reflux for 18 hours, cooled and filtered. The carbon tetrachloride filtrate is concentrated under reduced pressure to give a deep orange liquid. Vacuum distillation at 115°-120° C. (0.5 mm) gives ethyl α-bromo-3,4-dichlorophenylacetate as a pale yellow liquid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04231935
출처 데이터셋uspto-grants-1980_11
ORD IDord-c4fd411efeeb4b9db9e34fe4dd144fcb
출처 메모uspto-grants-1980_11