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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1192789Generated: October 26, 2026

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

https://huagongshe.com/reaction/1192789

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 numberUS08680269B2
Source datasetuspto-grants-2014_03
ORD IDord-ff065cca4b164695b603c70faad64bfd
Source noteuspto-grants-2014_03