Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1893476Generated: October 30, 2026

Imidazole → HCID 59333299, compound

https://huagongshe.com/reaction/1893476

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantDiisopropylethylamineHCID 81531—
Reactant1-Bromo-5-fluoro-4-nitro-2-(trifluoromethyl)benzeneHCID 59419785—
SolventAcetonitrileHCID 6342—
ProductHCID 59333299HCID 5933329986.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 1-bromo-5-fluoro-4-nitro-2-(trifluoromethyl)benzene (16.0 g, 0.0556 mol), imidazole (4.0 g, 0.0588 mol) and N,N-diisopropylethylamine (10.1 mL, 0.0582 mol) in acetonitrile (160 mL) is stirred under nitrogen for 1.5 hour at 80° C. After concentration of the reaction mixture, the residue is partitioned between water and ethyl acetate. The aqueous phase is extracted with ethyl acetate, the combined organic phases are washed in turn with a saturated solution of ammonium chloride, brine and dried over sodium sulfate. Concentration and purification by cake filtration over silica gel, eluting with a mixture of ethyl acetate and cyclohexane from 2/8 to 1/1 affords the title compound as a yellow solid (16.1 g, 86.2%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513250B2
Source datasetuspto-grants-2013_08
ORD IDord-4242963cda404db48465ed51562c1e37
Source noteuspto-grants-2013_08