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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242254Generated: October 27, 2026

Ethyl bromoacetate → ethyl 2-(4-cyano-1H-imidazol-1-yl)acetate

https://huagongshe.com/reaction/242254

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium ethoxideHCID 2723922—
ReactantHCID 178510437HCID 178510437—
SolventEthanolHCID 702—
Productethyl 2-(4-cyano-1H-imidazol-1-yl)acetateHCID 68753735—

Reaction Steps

3.3 g (35.3 mmol) 1H-imidazole-4-carbonitrile [Matthews et al., J. Org. Chem. 1986, 51, 3228-3231] are initially introduced into 13.2 ml (11.5 g, 35.3 mmol) 21% strength sodium ethylate solution in ethanol and 4.3 ml (6.5 g, 38.9 mmol) ethyl bromoacetate are added. The reaction mixture is stirred at RT for 16 h. For working up, the solid which has precipitated out is filtered off, the residue on the filter is washed with ethanol and the filtrate is concentrated in vacuo. Diisopropyl ether is added to the residue, the mixture is filtered again, the filtrate is concentrated again on a rotary evaporator and the residue is dried in vacuo.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653111B2
Source datasetuspto-grants-2014_02
ORD IDord-cf7ef924dc23455a9eb63ec62f4e3ee7
Source noteuspto-grants-2014_02