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HRID 2166341作成日:2026年10月27日

Ethyl bromoacetate → HCID 15269110、化合物

https://huagongshe.com/reaction/2166341

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl bromoacetateHCID 7748—
反応物4-(4-Chlorophenyl)-2-pyrrolidinoneHCID 185490—
反応物SodiumHCID 5360545—
溶媒EthanolHCID 702—
生成物HCID 15269110HCID 15269110—

反応手順

13 g (565 mmol) of sodium are added in portions to 410 ml of ethanol. After it has dissolved completely, 107 g (545 mmol) of 4-(p-chlorophenyl)-2-oxopyrrolidine are added, the whole is stirred at room temperature for 2 hours, concentrated to dryness by evaporation under reduced pressure and dried overnight at 100° under reduced pressure. The resulting sodium 4-(p-chlorophenyl)-2-oxopyrrolidine is made into a slurry in 340 ml of toluene, and a solution of 63.7 ml (95.9 g; 574 mmol) of bromoacetic acid ethyl ester is added dropwise, while stirring, at 20° to 25°. The whole is stirred for a further 16 hours, concentrated to dryness by evaporation under reduced pressure at approximately 70° and partitioned between 300 ml of water and 600 ml of ethyl acetate. The organic phase is separated off, washed with saturated sodium chloride solution, dried over sodium sulphate, filtered and concentrated to dryness by evaporation under reduced pressure. 2-[4-(p-chlorophenyl)-2-oxopyrrolidin-1-yl]-acetic acid ethyl ester is obtained which, for purification, is distilled under reduced pressure; b.p.=176°-178° at 0.02 torr (0.027 mbar).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04945092
出典データセットuspto-grants-1990_07
ORD IDord-adddd17015a244b4afd7eaf2d6ad110c
出典メモuspto-grants-1990_07