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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1758837Generated: November 1, 2026

Dicyclohexylcarbodiimide → N-(1-Carboxyethyl)-L-alanyl-L-proline

https://huagongshe.com/reaction/1758837

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantProline benzyl ester hydrochlorideHCID 2733413—
ReactantHCID 54011285HCID 54011285—
ReactantHCID 54407250HCID 54407250—
SolventPyridineHCID 1049—
SolventTriethylamineHCID 8471—
ProductN-(1-Carboxyethyl)-L-alanyl-L-prolineHCID 53882949—

Reaction Steps

Dissolve 0.75 g of N-(1-carbobenzoxyethyl)-L-alanine in pyridine and add 7.5 ml of 1 M triethylamine in pyridine. Cool, and add 1.09 g L-proline benzyl ester hydrochloride and 0.678 g dicyclohexylcarbodiimide. Store at 0° C. for 20 hours. Filter, then concentrate the reaction mixture in vacuo. Dissolve the residue in ethyl acetate and wash this solution with saturated K2CO3, then brine. Dry the organic phase, concentrate in vacuo, then chromatograph the residue on silica gel with ethyl acetate-hexane to isolate the diastereoisomeric mixture of N-(1-carbobenzoxyethyl)-L-alanyl-L-proline.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04374829
Source datasetuspto-grants-1983_02
ORD IDord-82f6eee09e4f489f9c5ad9d8d6f68716
Source noteuspto-grants-1983_02