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HRID 19256作成日:2026年10月26日

Benzoyl Peroxide → (E)-4-bromo-3-(3-bromo-phenoxy)-but-2-enoic acid ethyl ester

https://huagongshe.com/reaction/19256

反応式

関与物質

役割名称HCID仕込み量
反応物Benzoyl PeroxideHCID 7187—
反応物N-bromobutanimideHCID 67184—
反応物(E)-3-(3-bromo-phenoxy)-but-2-enoic acid ethyl esterHCID 66895334—
溶媒Carbon TetrachlorideHCID 5943—
生成物(E)-4-bromo-3-(3-bromo-phenoxy)-but-2-enoic acid ethyl esterHCID 6689374431.6%

反応手順

To a stirred mixture of (E)-3-(3-bromo-phenoxy)-but-2-enoic acid ethyl ester (5.80 g, 0.020 mol) in carbon tetrachloride (30 mL) under a nitrogen atmosphere was added N-bromosuccinimide (5.51 g, 0.031 mol) and benzoyl peroxide (500 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-(3-bromo-phenoxy)-but-2-enoic acid ethyl ester (2.30 g, 31%) as a yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07741327B2
出典データセットuspto-grants-2010_06
ORD IDord-b7d634ae72814e9599086035e6f89c16
出典メモuspto-grants-2010_06