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HRID 601729作成日:2026年10月26日

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

https://huagongshe.com/reaction/601729

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物1-Phenethylamine, (+)-HCID 643189—
反応物2-(2-Oxopyrrolidin-1-yl)butanoic acidHCID 10464751—
溶媒TolueneHCID 1140—
生成物(R)-1-Phenylethanamine (S)-2-(2-oxopyrrolidin-1-yl)butanoateHCID 4414030397.8%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07902380B2
出典データセットuspto-grants-2011_03
ORD IDord-f6523e3307784bdab6a95afdba9aa4d4
出典メモuspto-grants-2011_03