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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2268278Generated: October 26, 2026

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

https://huagongshe.com/reaction/2268278

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 numberUS06326500B1
Source datasetuspto-grants-2001_12
ORD IDord-deb34f08870d41e5a43bf157f740e15d
Source noteuspto-grants-2001_12