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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2166341생성일: 2026년 10월 27일

Ethyl bromoacetate → HCID 15269110, 화합물

https://huagongshe.com/reaction/2166341

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl bromoacetateHCID 7748—
반응물4-(4-Chlorophenyl)-2-pyrrolidinoneHCID 185490—
반응물SodiumHCID 5360545—
용매EthanolHCID 702—
생성물HCID 15269110HCID 15269110—

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04945092
출처 데이터셋uspto-grants-1990_07
ORD IDord-adddd17015a244b4afd7eaf2d6ad110c
출처 메모uspto-grants-1990_07