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HRID 224289作成日:2026年10月25日

Benzoyl Peroxide → Ethyl 2-bromo-2-(3,4-dichlorophenyl)acetate

https://huagongshe.com/reaction/224289

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Ethyl 3,4-dichlorophenylacetateHCID 2737422—
溶媒Carbon TetrachlorideHCID 5943—
生成物Ethyl 2-bromo-2-(3,4-dichlorophenyl)acetateHCID 12717583—

反応手順

In a three-necked flask fitted with a Nichrome stirrer and a reflux condenser is placed 7.0 g of ethyl 3,4-dichlorophenylacetate, 5.9 g of N-bromosuccinimide, 0.1 g of benzoyl peroxide and 150 ml of carbon tetrachloride. The reaction mixture is heated at reflux for 18 hours, cooled and filtered. The carbon tetrachloride filtrate is concentrated under reduced pressure to give a deep orange liquid. Vacuum distillation at 115°-120° C. (0.5 mm) gives ethyl α-bromo-3,4-dichlorophenylacetate as a pale yellow liquid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04231935
出典データセットuspto-grants-1980_11
ORD IDord-c4fd411efeeb4b9db9e34fe4dd144fcb
出典メモuspto-grants-1980_11