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HRID 66285作成日:2026年10月26日

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

https://huagongshe.com/reaction/66285

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US04131611
出典データセットuspto-grants-1978_12
ORD IDord-8bb4d254d7f440ec8351d60f1eca7e2b
出典メモuspto-grants-1978_12