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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 876673Generated: October 30, 2026

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

https://huagongshe.com/reaction/876673

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 numberUS08987261B2
Source datasetuspto-grants-2015_03
ORD IDord-36ba3b0d5cf74d1a9e90194334b5512f
Source noteuspto-grants-2015_03