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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1733652Generated: October 25, 2026

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

https://huagongshe.com/reaction/1733652

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantBenzyloxycarbonyl-L-prolineHCID 101987—
ReactantL-Leucine, ethyl ester, hydrochloride (1:1)HCID 11658447—
ReactantEthyl cyano{[(methanesulfonyl)oxy]imino}acetateHCID 54531055—
SolventTriethylamineHCID 8471—
ProductEthyl N-(1-((benzyloxy)carbonyl)-L-prolyl)-L-leucinateHCID 645307540.9%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04242507
Source datasetuspto-grants-1980_12
ORD IDord-8efbbd2f237244b7b894d13b45c3f98b
Source noteuspto-grants-1980_12