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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1956888Generated: October 27, 2026

Diethyl Malonate → ethyl 2-carbethoxy-3-(1-benzyl-1H-imidazol-2-yl)propanoate

https://huagongshe.com/reaction/1956888

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl MalonateHCID 7761—
Reactant1-benzyl-2-(chloromethyl)-1H-imidazole hydrochlorideHCID 2779243—
ReactantSodiumHCID 5360545—
SolventEthanolHCID 702—
Productethyl 2-carbethoxy-3-(1-benzyl-1H-imidazol-2-yl)propanoateHCID 18349794—

Reaction Conditions

Temperature0 °C

Reaction Steps

Diethyl malonate (52.45 g) in ethanol (50 ml) was added dropwise to a solution of sodium (11.3 g) in dry ethanol (300 ml) with stirring. The mixture was cooled to 0° C. and a solution of 1-benzyl-2-chloromethylimidazole hydrochloride (40.0 g, prepared as described in J.A.C.S. 1949, 383) in dry ethanol (250 ml) was added over 30 minutes with stirring. The mixture was stirred at ambient temperature for 2 hours and then the ethanol removed under reduced pressure. Ice cold 2M hydrochloric acid (400 ml) was added to the residue and the mixture was washed with ether. The aqueous layer was basified with solid sodium carbonate and then extracted with dichloromethane to give ethyl 2-carbethoxy-3-(1-benzyl-1H-imidazol-2-yl)propanoate as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05780642
Source datasetuspto-grants-1998_07
ORD IDord-ab8ef9afd3e143dd965b363203a2b779
Source noteuspto-grants-1998_07