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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1418461Generated: October 25, 2026

4-Fluoroiodobenzene → 1-(4-iodophenyl)-2-methyl-1H-imidazole

https://huagongshe.com/reaction/1418461

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-FluoroiodobenzeneHCID 9605—
Reactant2-MethylimidazoleHCID 12749—
ReactantSodium hydrideHCID 24758—
SolventDimethylformamideHCID 6228—
Product1-(4-iodophenyl)-2-methyl-1H-imidazoleHCID 1128909051.4%

Reaction Steps

To a stirred solution of 2-methylimidazole (13.6 g, 165 mmol) in DMF (500 ml) was added sodium hydride (6.60 g, 165 mmol, 60% dispersion in mineral oil) in portions. The resulting white suspension was stirred at room temperature for 30 min, 4-fluoroiodobenzene (33.3 g, 150 mmol) added and the mixture heated at 100° C. After 16 hr, the bulk of DMF was removed by evaporation. The residue was then partitioned between a mixture of ethyl acetate-toluene (2:1, 500 ml) and water(250 ml). The organic layer was separated and washed with water (250 ml). Product was extracted with 10% aqueous hydrogen chloride (2×200 ml) and the combined aqueous extracts neutralized with 30% aqueous potassium hydroxide. The resulting suspension was extracted with a mixture of ethyl acetate-toluene (2:1, 3×250 ml) and the combined organic extracts washed with water (2×250 ml), brine (250 ml), dried (magnesium sulfate) and concentrated to dryness. The residue was recrystallized from toluene to afford the titled compound as off-white solids (21.9 g, 51%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05883106
Source datasetuspto-grants-1999_03
ORD IDord-8a3ef8ccbf4844dc8cb3b5b4c8a8d643
Source noteuspto-grants-1999_03