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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1597863Generated: October 30, 2026

Imidazole → 3-(1H-imidazol-1-yl)benzonitrile

https://huagongshe.com/reaction/1597863

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant3-FluorobenzonitrileHCID 67880—
CatalystCopperHCID 23978—
SolventDimethylformamideHCID 6228—
Product3-(1H-imidazol-1-yl)benzonitrileHCID 496127247.1%

Reaction Steps

A mixture of 3-fluorobenzonitrile (18 ml, 168.38 mmol), imidazole (11.46 g), K2CO3 (25.59 g), copper (1.75 g), potassium iodide (1.75 g) and DMF (125 ml) was refluxed overnight. The reaction mixture was cooled to room temperature and poured into ice/water (600 ml). A precipitate formed, which was collected by filtration, washed with water, dissolved in ethanol (25 ml)/CHCl3 (500 ml) and filtered. The filtrates were partitioned in water, the organic layer was separated, dried over MgSO4 and stripped. The residue was combined with the product from another experimental run and was recrystallized from CHCl3 /hexanes to afford 13.4 g of 3-(1-imidazolyl)benzonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05736548
Source datasetuspto-grants-1998_04
ORD IDord-bf909b1aa5c94c218cfbcbc1d7a09b44
Source noteuspto-grants-1998_04