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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 19290생성일: 2026년 10월 24일

Benzoyl Peroxide → (E)-4-bromo-3-(6-methyl-pyridin-3-yloxy)-but-2-enoic acid ethyl ester

https://huagongshe.com/ko/reaction/19290

반응식

참여 물질

역할이름HCID투입량
반응물Benzoyl PeroxideHCID 7187—
반응물N-bromobutanimideHCID 67184—
반응물(E)-3-(6-methyl-pyridin-3-yloxy)-but-2-enoic acid ethyl esterHCID 66893705—
용매Carbon TetrachlorideHCID 5943—
생성물(E)-4-bromo-3-(6-methyl-pyridin-3-yloxy)-but-2-enoic acid ethyl esterHCID 6689526344%

반응 단계

To a stirred mixture of (E)-3-(6-methyl-pyridin-3-yloxy)-but-2-enoic acid ethyl ester (3.50 g, 0.016 mol) in carbon tetrachloride (25 mL) under a nitrogen atmosphere was added N-bromosuccinimide (4.23 g, 0.024 mol) and benzoyl peroxide (383 mg, 0.002 mol). Nitrogen gas was bubbled through the mixture for 5 min, and the resulting mixture was heated to reflux for 4 h. The reaction mixture was then placed in the refrigerator overnight. The solids formed were removed by filtration and the filtrate concentrated in vacuo. The crude product obtained was purified using flash column chromatography (silica gel (100-200 mesh), ethyl acetate/hexanes) to afford (E)-4-bromo-3-(6-methyl-pyridin-3-yloxy)-but-2-enoic acid ethyl ester (2.10 g, 44%) as a yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741327B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-57f19c9e0484430786959c3b60c94e7e
출처 메모uspto-grants-2010_06