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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1439966Erstellt: 27. Oktober 2026

Dimethylformamide → (S)-Benzyl (2-oxotetrahydrofuran-3-yl)carbamate

https://huagongshe.com/reaction/1439966

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylformamideHCID 6228—
Edukt1-HydroxybenzotriazoleHCID 75771—
EduktCbz-L-HomoserineHCID 489187—
Edukt1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
LösungsmittelWaterHCID 962—
Produkt(S)-Benzyl (2-oxotetrahydrofuran-3-yl)carbamateHCID 48918584,3%

Reaktionsschritte

A mixture of N-benzyloxycarbonyl-(L)-homoserine (9.0 g), 1-hydroxybenzotriazole (HOBt) (5.4 g) and N,N-dimethylformamide (DMF) (50 ml) was provided and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (WSCD.HCl) (7.5 g) was added to the mixture under ice-cooling. The whole mixture was stirred at room temperature for 14 hours. The reaction mixture was then poured into water and extracted with ethyl acetate. The ethyl acetate layer was washed with 1% aqueous citric acid, water, saturated aqueous sodium hydrogen carbonate and saturated aqueous sodium chloride in the order mentioned and dried over MgSO4 and the solvent was distilled off, whereby (S)-3-(N-benzyloxycarbonylamino)tetrahydrofuran-2-one (7.0 g, 84.3%) was obtained. This product was recrystallized from dichloromethane-isopropyl ether. Colorless needles, m.p. 129°-130° C. Optical rotation [α]D -0.5° (C=0.52, CHCl3).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05496834
Quelldatensatzuspto-grants-1996_03
ORD IDord-5eeee8c67d45497a852fd5dd5cfbdfa2
Quellennotizuspto-grants-1996_03