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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1260805Generated: November 2, 2026

Imidazole → 3-(1H-Imidazol-1-YL)-5-(trifluoromethyl)aniline

https://huagongshe.com/reaction/1260805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactant8-HydroxyquinolineHCID 1923—
ReactantPotassium CarbonateHCID 11430—
ReactantAmmonium HydroxideHCID 14923—
Reactant3-Bromo-5-(trifluoromethyl)anilineHCID 2735880—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product3-(1H-Imidazol-1-YL)-5-(trifluoromethyl)anilineHCID 4422263766.2%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 3-Amino-5-bromobenzotrifluoride (4.0 g, 0.0167 mol), 8-hydroxy quinoline (0.362 g, 0.0025 mol), CuI (0.476 g, 0.025 mol), imidazole (1.36 g, 0.0199 mol), and potassium carbonate (2.52 g, 0.0183 mol) in 17 mL of DMSO (degassed with argon for ˜10 min) was heated at 120° C. under an atmosphere of argon for 15 h; the HPLC indicated no starting material. A 14% aqueous solution of ammonium hydroxide was added to the cooled mixture and this was stirred for 1 h at ambient temperature. Water (50 mL) and EtOAc (200 mL) were added and the aqueous layer was extracted with EtOAc (3×30 mL). The combined organic layers were dried over Na2SO4 and concentrated. The crude product was purified by silica gel flash chromatography (eluted with EtOAc/hexanes) to provide 2.51 g of product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470851B2
Source datasetuspto-grants-2013_06
ORD IDord-aa3907566cc0434db55ac5b775d00915
Source noteuspto-grants-2013_06