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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2230243Erstellt: 24. Oktober 2026

Citric Acid → 1-Benzyl 3-ethyl 4-oxopyrrolidine-1,3-dicarboxylate

https://huagongshe.com/de/reaction/2230243

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCitric AcidHCID 311—
EduktEthyl AcrylateHCID 8821—
EduktN-((Phenylmethoxy)carbonyl)glycine ethyl esterHCID 14366—
EduktSodium hydrideHCID 24758—
LösungsmittelTolueneHCID 1140—
LösungsmittelEthyl AcetateHCID 8857—
Produkt1-Benzyl 3-ethyl 4-oxopyrrolidine-1,3-dicarboxylateHCID 15043278—

Reaktionsschritte

Ethyl acrylate (65.01 ml, 600.0 mmol) was added to a toluene (1,200 ml) solution containing N-benzyloxycarbonylglycine ethyl ester (156.3 g, 600.0 mmol) and then, under ice-cooling, sodium hydride (60% oil; 26.40 g, 660.0 mmol) was added thereto. After 10 minutes of stirring at the same temperature, the ice bath was taken off, and the mixture was stirred at room temperature for 20 minutes and then at 50° C. for 3 hours. After completion of the reaction, and under ice-cooling, the reaction solution was adjusted to about pH 3 by adding 10% citric acid aqueous solution and mixed with ethyl acetate, and the mixture was shaken and then subjected to separation of layers. The organic layer was separated and washed with saturated brine, and the water layer was further extracted with ethyl acetate. The organic layers were dried over anhydrous sodium sulfate and then filtered, and the solvent was evaporated under a reduced pressure to obtain 196.7 g (600.0 mmol, quantitative) of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06423843B1
Quelldatensatzuspto-grants-2002_07
ORD IDord-181fde3ae9524a6095c42a2a2df0800b
Quellennotizuspto-grants-2002_07