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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1706496Generated: October 26, 2026

Dicyclohexylcarbodiimide → N-(4-methoxycarbonyl-2-methylbutanoyl)-L-alanine benzyl ester

https://huagongshe.com/reaction/1706496

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactantbenzyl (2S)-2-aminopropanoateHCID 726858—
Reactant4-Carbomethoxy-2-methylbutanoic acidHCID 13192897—
ReactantHCID 178418300HCID 178418300—
SolventDichloromethaneHCID 6344—
ProductN-(4-methoxycarbonyl-2-methylbutanoyl)-L-alanine benzyl esterHCID 22804619—

Reaction Steps

4-methoxycarbonyl-2-methylbutanoic acid (3.1 g.), L-alanine benzyl ester (3.58 g.) and hydroxybenzotriazole (2.7 g.) are dissolved in dichloromethane. The solution is chilled in the ice bath and dicyclohexylcarbodiimide (4.12 g.) is added. After stirring 15 minutes in the ice bath and 18 hours at room temperature the precipitate is filtered off and the filtrate is concentrated to dryness. The residue is dissolved in ethyl acetate and washed neutral. The organic phase is dried over magnesium sulfate and concentrated to dryness to yield N-(4-methoxycarbonyl-2-methylbutanoyl)-L-alanine benzyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04207342
Source datasetuspto-grants-1980_06
ORD IDord-c3274b9e92d143f2b6991e3dba7e5626
Source noteuspto-grants-1980_06