Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 708945Generated: October 26, 2026

8-Hydroxyquinoline → 4-bromo-1-(4-(trifluoromethoxy)phenyl)-1H-imidazole

https://huagongshe.com/reaction/708945

Reaction equation

Participants

RoleNameHCIDCharge
Reactant8-HydroxyquinolineHCID 1923—
ReactantCesium carbonateHCID 10796—
Reactant1-Iodo-4-(trifluoromethoxy)benzeneHCID 2777294—
ReactantHCID 178418934HCID 178418934—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product4-bromo-1-(4-(trifluoromethoxy)phenyl)-1H-imidazoleHCID 5782443551.3%

Reaction Conditions

Temperature130 °C

Reaction Steps

A round bottom flask was charged with 4-bromoimidazole (1.15 g, 7.81 mmol), CuI (0.07 g, 0.36 mmol), 8-hydroxyquinoline (0.05 g, 0.36 mmol), cesium carbonate (3.39 g, 10.4 mmol) and 4-trifluoromethoxyiodobenzene (1.50 g, 5.21 mmol). A 10:1 mixture of DMF (15 mL) and H2O (1.5 mL) was added to the reaction mixture, and the solution was heated to 130° C. for 4 h. The reaction mixture was then diluted with EtOAc and washed sequentially with H2O, ammonium chloride (NH4Cl, saturated), H2O and sodium bicarbonate (NaHCO3). The organics were dried over MgSO4, filtered and purified by reverse phase column chromatography to give the imidazole (820 mg) as a white solid: mp 139-141° C.; ESIMS m/z 308.0 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09179681B2
Source datasetuspto-grants-2015_11
ORD IDord-610b699d9a7e41c1ba04864d1c1f106a
Source noteuspto-grants-2015_11