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HRID 901154作成日:2026年10月25日

Water → 3-Benzoyloxy-4-chlorobenzyl bromide

https://huagongshe.com/reaction/901154

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Benzoyl PeroxideHCID 7187—
反応物N-bromobutanimideHCID 67184—
反応物3-Benzoyloxy-4-chlorotolueneHCID 16749222—
溶媒Diethyl EtherHCID 3283—
溶媒Carbon TetrachlorideHCID 5943—
生成物3-Benzoyloxy-4-chlorobenzyl bromideHCID 16747840—

反応手順

A mixture of benzoic acid 2-chloro-5-methyl-phenyl ester (CAB02124, 2.47 g, 10.0 mmol), N-bromo-succinimide (1.96 g, 11.0 mmol) and dibenzoyl peroxide (10 mg) in carbon tetrachloride (25 mL) was heated to reflux for 1 hour (TLC-control). After cooling to room temperature water (50 mL) and diethyl ether (100 mL) were added. The organic layer was separated, washed with brine (20 mL), dried over sodium sulphate and concentrated under reduced pressure. The residue was purified by column chromatography (EtOAc:hexane, 1:40, Rf: 0.21). Yield: 2.012 g (62%) colourless oil, which solidified after a few hours (contains ca. 10% benzoic acid 5-dibromomethyl-2-chloro-phenyl ester).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07361677B2
出典データセットuspto-grants-2008_04
ORD IDord-4579a21d5d1c450ab350e72cee382f06
出典メモuspto-grants-2008_04