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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1733652Erstellt: 24. Oktober 2026

Chloroform → Ethyl N-(1-((benzyloxy)carbonyl)-L-prolyl)-L-leucinate

https://huagongshe.com/de/reaction/1733652

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChloroformHCID 6212—
EduktBenzyloxycarbonyl-L-prolineHCID 101987—
EduktL-Leucine, ethyl ester, hydrochloride (1:1)HCID 11658447—
EduktEthyl cyano{[(methanesulfonyl)oxy]imino}acetateHCID 54531055—
LösungsmittelTriethylamineHCID 8471—
ProduktEthyl N-(1-((benzyloxy)carbonyl)-L-prolyl)-L-leucinateHCID 645307540,9%

Reaktionsschritte

N-Benzyloxycarbonyl-L-proline (1.25 g) and L-leucine ethyl ester hydrochloride (1.0 g) are suspended into chloroform (10 ml), and therein is dissolved triethylamine (1.40 ml). To the solution is added ethyl 2-methanesulfonyloxyimino-2-cyanoacetate (1.1 g) and the mixture is stirred at room temperature for 16 hours. After reaction, the reaction mixture is extracted with ethyl acetate. The extract is washed with water, 1 N aqueous sodium hydrogen carbonate, water, 1 N hydrochloric acid and water in order and then dried over anhydrous magnesium sulfate. After drying, the solvent is distilled off and the resulting residue is crystallized from petroleum ether to give N-(N-benzyloxycarbonyl-L-prolyl)-L-leucine ethyl ester (0.8 g), melting point: 65°-67° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04242507
Quelldatensatzuspto-grants-1980_12
ORD IDord-8efbbd2f237244b7b894d13b45c3f98b
Quellennotizuspto-grants-1980_12