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HRID 19048作成日:2026年10月26日

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

https://huagongshe.com/reaction/19048

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3-(3-Trifluoromethyl-phenoxy)-but-2-enoic acid ethyl esterHCID 66894464—
溶媒Carbon TetrachlorideHCID 5943—
生成物4-Bromo-3-(3-trifluoromethyl-phenoxy)-but-2-enoic acid ethyl esterHCID 6689460183.1%

反応条件

温度25 °C

反応手順

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.

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-d9819244923144d88700afc54e615dea
出典メモuspto-grants-2010_06