돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 19048생성일: 2026년 10월 24일

Benzoyl Peroxide → 4-Bromo-3-(3-trifluoromethyl-phenoxy)-but-2-enoic acid ethyl ester

https://huagongshe.com/ko/reaction/19048

반응식

참여 물질

역할이름HCID투입량
반응물Benzoyl PeroxideHCID 7187—
반응물N-bromobutanimideHCID 67184—
반응물3-(3-Trifluoromethyl-phenoxy)-but-2-enoic acid ethyl esterHCID 66894464—
용매Carbon TetrachlorideHCID 5943—
생성물4-Bromo-3-(3-trifluoromethyl-phenoxy)-but-2-enoic acid ethyl esterHCID 6689460183.1%

반응 조건

온도25 °C

반응 단계

A solution of 3-(3-trifluoromethyl-phenoxy)-but-2-enoic acid ethyl ester (1.31 g, 4.77 mmol) in carbon tetrachloride (25 mL) was treated with N-bromosuccinimide (0.94 g, 5.28 mmol) and benzoyl peroxide (0.12 g). The reaction was then warmed to reflux for 5 h. At this time, the reaction was cooled to 25° C. and then placed in the freezer over the weekend. At this time, the reaction was removed from the freezer and allowed to thaw. The resulting precipitate was removed by filtration. The filtrate was concentrated in vacuo. Purification by Analogix flash chromatography (40 g, 1-10% ethyl acetate/hexanes) afforded impure 4-bromo-3-(3-trifluoromethyl-phenoxy)-but-2-enoic acid ethyl ester (1.40 g, 83%) as a pale, yellow oil. The material was used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741327B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-d9819244923144d88700afc54e615dea
출처 메모uspto-grants-2010_06