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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1511792Erstellt: 27. Oktober 2026

Acetic Acid → (3R*,4S*)-4-Benzylamino-pyrrolidine-1,3-dicarboxylic acid 1-tert-butyl ester 3-ethyl ester

https://huagongshe.com/reaction/1511792

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktBenzylamineHCID 7504—
EduktSodium cyanoborohydrideHCID 5003444—
Edukt1-tert-Butyl 3-ethyl 4-oxopyrrolidine-1,3-dicarboxylateHCID 10868942—
LösungsmittelEthanolHCID 702—
Produkt(3R*,4S*)-4-Benzylamino-pyrrolidine-1,3-dicarboxylic acid 1-tert-butyl ester 3-ethyl esterHCID 6802862254%

Reaktionsschritte

To a solution of (RS)-4-oxo-pyrrolidine-1,3-dicarboxylic acid 1-tert-butyl ester 3-ethyl ester (commercial; 1 g, 3.9 mmol) in EtOH (15 mL) were added benzylamine (0.85 mL, 7.77 mmol) and AcOH (0.45 mL, 7.77 mmol) and the mixture was stirred 3 h at rt. Sodium cyanoborohydride (0.98 g, 15.5 mmol) was then added at rt and the mixture was heated to 75° C. for 5 h, then 15 h to 50° C. and again 1 h to 75° C. The mixture was concentrated under reduced pressure, water was added and the mixture extracted 3× with EA. The combined org. extracts were washed with brine dried over MgSO4 and concentrated under reduced pressure. The residue was purified by CC (Hep/EA from 2:1 to 1:1) to afford the title intermediate as a yellow oil (0.73 g, 54%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08217029B2
Quelldatensatzuspto-grants-2012_07
ORD IDord-48dd7f9be9884fb39e7af3737731e561
Quellennotizuspto-grants-2012_07