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HRID 19217作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/19217

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-(2-t-butyl-phenoxy)-but-2-enoic acid ethyl esterHCID 67504254—
溶媒Carbon TetrachlorideHCID 5943—
生成物(E)-4-bromo-3-(2-t-butyl-phenoxy)-but-2-enoic acid ethyl esterHCID 6750452251.3%

反応手順

To a stirred mixture of (E)-3-(2-t-butyl-phenoxy)-but-2-enoic acid ethyl ester (3.20 g, 0.012 mol) in carbon tetrachloride (20 mL) under a nitrogen atmosphere was added N-bromosuccinimide (3.26 g, 0.018 mol) and benzoyl peroxide (295 mg, 0.001 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-(2-t-butyl-phenoxy)-but-2-enoic acid ethyl ester (2.10 g, 50%) 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-bb3f25397f944f85a7a90471a6a73096
出典メモuspto-grants-2010_06