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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2366880Generated: October 31, 2026

p-Fluoronitrobenzene → ethyl 1-(4-nitrophenyl)-1H-imidazole-4-carboxylate

https://huagongshe.com/reaction/2366880

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-FluoronitrobenzeneHCID 9590—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 178469898HCID 178469898—
SolventAcetonitrileHCID 6342—
Productethyl 1-(4-nitrophenyl)-1H-imidazole-4-carboxylateHCID 1872677384.1%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of ethyl 1H-imidazole-4-carboxylate (8 g, 57.1 mmol), 4-fluoro-1-nitrobenzene (8.05 g, 57.1 mmol) and potassium carbonate (8.68 g, 62.8 mmol) in acetonitrile (100 mL) was stirred at 60° C. for 16 h then cooled to room temperature and most the solvent was removed in vacuo. The residue was partitioned between AcOEt (200 mL) and water (150 mL) and the layers were separated. The organic phase was dried over MgSO4 and concentrated in vacuo. Purification of the residue by flash chromatography on silica gel (gradient: 0 to 5% MeOH in DCM) gave ethyl 1-(4-nitrophenyl)-1H-imidazole-4-carboxylate (12.53 g, 48.0 mmol, 84%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697725B2
Source datasetuspto-grants-2014_04
ORD IDord-8a8af0830f3d4e42be10cc3378a45794
Source noteuspto-grants-2014_04