Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1916376Generated: November 1, 2026

Ethyl chloroacetate → ethyl (2-formyl-1H-imidazol-1-yl)acetate

https://huagongshe.com/reaction/1916376

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroacetateHCID 7751—
ReactantPotassium CarbonateHCID 11430—
ReactantN-methyl-2-pyrrolidoneHCID 13387—
Reactant1H-imidazole-2-carbaldehydeHCID 24955—
SolventWaterHCID 962—
Productethyl (2-formyl-1H-imidazol-1-yl)acetateHCID 62222097—

Reaction Steps

To 1H-imidazole-2-carboaldehyde (2.0 g), N-methylpyrrolidone (25 mL) was added, followed by dissolution with heating. To the resultant solution, ethyl chloroacetate (11.1 mL) and potassium carbonate (2.9 g) were added. The reaction solution was stirred at room temperature for 14 hours. To the reaction solution, water (30 mL) was added. The aqueous layer was extracted twice with ethyl acetate. The organic layers were combined, washed with saturated saline and then dried over anhydrous sodium sulfate. The anhydrous sodium sulfate was removed by filtration and the solvent was concentrated under reduced pressure. The residue was purified by silica gel chromatography (dichloromethane) to obtain the title compound having the following physical properties (1.3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618122B2
Source datasetuspto-grants-2013_12
ORD IDord-0565e269818249d3a4ce5913ed66a94e
Source noteuspto-grants-2013_12