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HRID 278159作成日:2026年10月25日

Benzoyl Peroxide → 4-Cyano-3-fluorobenzyl bromide

https://huagongshe.com/reaction/278159

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2-Fluoro-4-methylbenzonitrileHCID 2778443—
溶媒Carbon TetrachlorideHCID 5943—
生成物4-Cyano-3-fluorobenzyl bromideHCID 2778466—

反応手順

To a solution of the product from Step C (22.2 g, 165 mmol) in 220 mL of carbontetrachloride was added N-bromosuccinimide (29.2 g, 164 mmol) and benzoylperoxide (1.1 g). The reaction was heated to reflux for 30 minutes, then cooled to room temperature. The solution was concentrated in vacuo to one-third the original volume, poured into EtOAc, washed with water, sat. aq. NaHCO3, and brine, then dried (Na2SO4), filtered, and concentrated in vacuo to provide the crude product. Analysis by 1H NMR indicated only partial conversion, so the crude material was resubjected to the same reaction conditions for 2.5 hours, using 18 g (102 mmol) of N-bromosuccinimide. After workup, the crude material was purified by silica gel chromatography (0-10% EtOAc/hexane) to provide the desired product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06358985B1
出典データセットuspto-grants-2002_03
ORD IDord-0820a53ea7a745d798d5c82f7b972f94
出典メモuspto-grants-2002_03