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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 601729생성일: 2026년 10월 25일

Triethylamine → (R)-1-Phenylethanamine (S)-2-(2-oxopyrrolidin-1-yl)butanoate

https://huagongshe.com/reaction/601729

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물1-Phenethylamine, (+)-HCID 643189—
반응물2-(2-Oxopyrrolidin-1-yl)butanoic acidHCID 10464751—
용매TolueneHCID 1140—
생성물(R)-1-Phenylethanamine (S)-2-(2-oxopyrrolidin-1-yl)butanoateHCID 4414030397.8%

반응 단계

A solution of (R)-alpha-methylbenzylamine (106 g) and triethylamine (89 g) in toluene (100 ml) was added to a suspension of (RS)-alpha-ethyl-2-oxo-1-pyrrolidineacetic acid (300 g, 1.75 mol) in toluene (1 L). The mixture was heated until complete dissolution, cooled to room temperature and stirred for 3 hours. The solids were filtered and rinsed with toluene (300 ml) to give 250 g of (s)-alpha-ethyl-2-oxo-1-pyrrolidineacetic acid (R)-alpha-methylbenzylamine salt. The solids were crystallized from toluene and 205 g (yield 41%) of (S)-alpha-ethyl-2-oxo-1-pyrrolidineacetic acid (R)-alpha-methylbenzylamine salt was obtained. The isolated solid was treated with hydrochloric acid solution and the enantiomerically pure (S)-alpha-ethyl-2-oxo-1-pyrrolidineacetic acid could be isolated in 90% yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07902380B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-f6523e3307784bdab6a95afdba9aa4d4
출처 메모uspto-grants-2011_03