戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 464997作成日:2026年10月25日

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

https://huagongshe.com/reaction/464997

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolamineHCID 700—
反応物Methyl 1-benzyl-5-oxopyrrolidine-3-carboxylateHCID 98909—
溶媒MethanolHCID 887—
生成物N-(2-hydroxyethyl)-5-oxo-1-(phenylmethyl)-3-pyrrolidinecarboxamideHCID 1428088391.3%

反応手順

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) 2-aminoethanol and 500 ml methanol were 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 1 N 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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04550104
出典データセットuspto-grants-1985_10
ORD IDord-0028cf40ed30490fb01a61e1b8f3ef59
出典メモuspto-grants-1985_10