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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 601729Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/601729

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt1-Phenethylamine, (+)-HCID 643189—
Edukt2-(2-Oxopyrrolidin-1-yl)butanoic acidHCID 10464751—
LösungsmittelTolueneHCID 1140—
Produkt(R)-1-Phenylethanamine (S)-2-(2-oxopyrrolidin-1-yl)butanoateHCID 4414030397,8%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07902380B2
Quelldatensatzuspto-grants-2011_03
ORD IDord-f6523e3307784bdab6a95afdba9aa4d4
Quellennotizuspto-grants-2011_03