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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582335Generated: November 1, 2026

2-Methylimidazole → 1-(2-fluoro-4-nitrophenyl)-2-methyl-1H-imidazole

https://huagongshe.com/reaction/1582335

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethylimidazoleHCID 12749—
ReactantDiisopropylethylamineHCID 81531—
Reactant1,2-Difluoro-4-nitrobenzeneHCID 123053—
SolventAcetonitrileHCID 6342—
Product1-(2-fluoro-4-nitrophenyl)-2-methyl-1H-imidazoleHCID 2187664552%

Reaction Steps

2-Methylimidazole (9.02 g, 0.11 M) and N,N-diisopropylethylamine (32.2 g, 0.25 M) were dissolved in acetonitrile (160 ml), and 3,4-difluoronitrobenzene (15.9 g, 0.1 M) added. The mixture was stirred and heated to reflux under nitrogen for 24 hours. Solvent was evaporated, the residue dissolved in ethyl acetate (300 ml), washed with water (150 ml), brine (150 ml), and dried (magnesium sulfate). The residue was recrystallised from a mixture of ethyl acetate (25 ml) and cyclohexane (150 ml) with the addition of charcoal to give the title compound (11.5 g), mp 106-107°. NMR(DMSO-d6) δ: 2.25 (s, 3H), 7.00 (d, 1H); 7.35 (t, 1H); 7.87 (t, 1H); 8.23 (dd, 1H); 8.43 (dd, 1H). MS (ESP): 222 (MH+) for C10H8FN3O 2

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06734200B1
Source datasetuspto-grants-2004_05
ORD IDord-dafa3cd2cd104e68874d13cacd9b1373
Source noteuspto-grants-2004_05