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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2051349Generated: November 2, 2026

1,1'-Carbonyldiimidazole → Glycine, N-(3-(2-(4-(acetylamino)-1-oxobutyl)-5-chlorophenyl)-1-oxopropyl)-, ethyl ester

https://huagongshe.com/reaction/2051349

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantDiisopropylethylamineHCID 81531—
ReactantGlycine ethyl ester, hydrochlorideHCID 2723640—
Reactant2-(4-Acetamidobutyryl)-5-chlorohydrocinnamic acidHCID 19833127—
SolventTetrahydrofuranHCID 8028—
ProductGlycine, N-(3-(2-(4-(acetylamino)-1-oxobutyl)-5-chlorophenyl)-1-oxopropyl)-, ethyl esterHCID 3078712—

Reaction Steps

1.75 g (0.006 mol) of 2-(4-acetamidobutyryl)-5-chlorohydrocinnamic acid and 0.95 g (0.006 mol) of 1,1'-carbonyldiimidazole are stirred at room temperature in 15 ml of tetrahydrofuran and 1.0 ml (0.006 mol) of N-ethyldiisopropylamine and 0.82 g (0.006 mol) of ethyl glycinate hydrochloride are then added thereto. After stirring at room temperature for 1 hour, the solution is concentrated, extracted with methylene chloride/water, dried with magnesium sulfate and the solvent is distilled in a vacuum. Chromatography on aluminum oxide with ethyl acetate-ethanol (9:1) and crystallization from methylene chloride/t-butyl methyl ether gives ethyl N-[2-(4-acetamidobutyryl)-5-chlorohydrocinnamoyl]-glycinate as white crystals with melting point 96°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05017608
Source datasetuspto-grants-1991_05
ORD IDord-3c8b3d0f76614deabc2bf4bf6a49daea
Source noteuspto-grants-1991_05