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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464006Generated: October 29, 2026

Triethylamine → N-(p-Chlorobenzoyl)-2-(2-cyanoethyl)alanine methyl ester

https://huagongshe.com/reaction/464006

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Chlorobenzoyl chlorideHCID 8501—
ReactantN-(N-benzyloxycarbonyl-L-prolyl)-2-(2-cyanoethyl)alanine methyl esterHCID 54540171—
SolventDichloromethaneHCID 6344—
ProductN-(p-Chlorobenzoyl)-2-(2-cyanoethyl)alanine methyl esterHCID 53771201—
ProductN-(N-benzyloxycarbonyl-L-prolyl)-2-(2-cyanoethyl)alanine methyl esterHCID 54540171—

Reaction Steps

p-Chlorobenzoyl chloride (0.91 g) and triethylamine (0.91 ml) were added at 5° C. to a solution of 0.85 g of isomer (i) of the 2-(2-cyanoethyl)alanine methyl ester in dichloromethane (20 ml), and the resulting mixture was stirred at 0°-5° C. for 2 hours. The reaction mixture was then washed with water (20 ml) and the organic layer was dried over magnesium sulphate. The solvent was distilled off and the residue was purified by silica gel Lobar column chromatography (eluent: 1/1 cyclohexane/ethyl acetate; flow rate: 12 ml/minute), giving 1.13 g of isomer (i) of the desired product as a colourless powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04545942
Source datasetuspto-grants-1985_10
ORD IDord-6f44b58168394d25b36cbdea420b052c
Source noteuspto-grants-1985_10