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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1189499Generated: October 27, 2026

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

https://huagongshe.com/reaction/1189499

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 water, ammonium chloride (saturated), water and sodium bicarbonate. The organics were dried over MgSO4, filtered and purified on a reverse phase column 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 numberUS08674109B2
Source datasetuspto-grants-2014_03
ORD IDord-9eb5a16a847c4f4fafa2e54540c7f8c0
Source noteuspto-grants-2014_03