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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 620859생성일: 2026년 10월 26일

Ethanolamine → N-(2-hydroxyethyl)-5-oxo-1-(phenylmethyl)-3-pyrrolidinecarboxamide

https://huagongshe.com/reaction/620859

반응식

참여 물질

역할이름HCID투입량
반응물EthanolamineHCID 700—
반응물Methyl 1-benzyl-5-oxopyrrolidine-3-carboxylateHCID 98909—
용매MethanolHCID 887—
생성물N-(2-hydroxyethyl)-5-oxo-1-(phenylmethyl)-3-pyrrolidinecarboxamideHCID 1428088391.3%

반응 단계

A mixture of 46.7 g (0.2 mole) of methyl 5-oxo-1-(phenylmethyl)-3-pyrrolidinecarboxylate [J. Org. Chem., 26, 1519 (1961)], 36.7 g (0.6 mole) of 2-aminoethanol and 500 ml methanol was refluxed overnight. The reaction was cooled to room temperature and the solvent removed at reduced pressure. The residue was taken up in dichloromethane and extracted 3×100 ml 1N sodium hydroxide. The aqueous layer was taken to pH 5, extracted 3×150 ml dichloromethane, then taken to pH 8 and again extracted 3×150 ml dichloromethane. The aqueous layer was concentrated at reduced pressure and the resulting slurry stirred in dichloromethane. The salts were filtered off. The combined organic layers were dried over magnesium sulfate, the solvent removed at reduced pressure to Yield 47.9 g of N-(2-hydroxyethyl)-5-oxo-1-(phenylmethyl)-3-pyrrolidinecarboxamide as an oil. This was used in the next step without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04822801
출처 데이터셋uspto-grants-1989_04
ORD IDord-8cffe67242db4981bc44b2bad854cb4e
출처 메모uspto-grants-1989_04