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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 242253Generated: October 31, 2026

Ethyl bromoacetate → [4-(Trifluoromethyl)-1H-imidazol-1-yl]acetic acid ethyl ester

https://huagongshe.com/reaction/242253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantSodium ethoxideHCID 2723922—
ReactantHCID 178418921HCID 178418921—
SolventEthanolHCID 702—
Product[4-(Trifluoromethyl)-1H-imidazol-1-yl]acetic acid ethyl esterHCID 59603647—

Reaction Steps

2.0 g (14.7 mmol) 4-(trifluoromethyl)-1H-imidazole are initially introduced into 5.5 ml (4.7 g, 14.7 mmol) 21% strength sodium ethylate solution in ethanol and 1.8 ml (2.7 g, 16.2 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. The product is obtained as a 9:1 mixture of the two regioisomers and is further reacted as such.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653111B2
Source datasetuspto-grants-2014_02
ORD IDord-f876192cd1d942caa0d27a280831bdda
Source noteuspto-grants-2014_02