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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 364047생성일: 2026년 10월 25일

Water → 2-(((1-Benzylpyrrolidin-3-yl)methyl)amino)ethanol

https://huagongshe.com/reaction/364047

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Sodium HydroxideHCID 14798—
반응물N-(2-hydroxyethyl)-5-oxo-1-(phenylmethyl)-3-pyrrolidinecarboxamideHCID 14280883—
반응물Aluminium lithium hydrideHCID 21226445—
용매TetrahydrofuranHCID 8028—
생성물2-(((1-Benzylpyrrolidin-3-yl)methyl)amino)ethanolHCID 1428088877.5%

반응 단계

A mixture of 46.66 g (0.178 mole) of N-(2-hydroxyethyl)-5-oxo-1-(phenylmethyl)-3-pyrrolidinecarboxamide in 200 ml of tetrahydrofuran was added dropwise to a slurry of 20.25 g (0.534 mole) of lithium aluminum hydride in 150 ml tetrahydrofuran. The reaction was refluxed three hours, then cooled in an ice bath. The work up consisted of sequential addition of 20 ml water, 20 ml 15% sodium hydroxide then 60 ml water. The reaction was filtered and the precipitate washed with ethanol. The filtrate was concentrated at reduced pressure, the residue taken up in dichloromethane, dried over magnesium sulfate, and the solvent removed at reduced pressure to give 32.31 g of 2-[[[1-(phenylmethyl)-3-pyrrolidinyl]methyl]amino]ethanol as an oil. This material was used in the next step without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04604401
출처 데이터셋uspto-grants-1986_08
ORD IDord-b9ddcc7b5ab5480b9ab5e3531e45c1e6
출처 메모uspto-grants-1986_08