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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1802626Generated: November 2, 2026

8-Hydroxyquinoline → (1-(3-fluoro-4-iodophenyl)-1H-imidazol-4-yl)methanol

https://huagongshe.com/reaction/1802626

Reaction equation

Participants

RoleNameHCIDCharge
Reactant8-HydroxyquinolineHCID 1923—
ReactantPotassium CarbonateHCID 11430—
Reactant2,5-DiiodofluorobenzeneHCID 2737096—
ReactantHCID 178418488HCID 178418488—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Product(1-(3-fluoro-4-iodophenyl)-1H-imidazol-4-yl)methanolHCID 66974146—

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of 2,5-diiodofluorobenzene II-4 (2.50 g, 7.18 mmol), 4-hydroxymethylimidazole hydrochloride (0.967 g, 7.18 mmol), 8-hydroxyquinoline (0.104 g, 0.717 mmol) and K2CO3 (2.00 g, 14.5 mmol) in DMSO (12 mL) was degassed with Ar before being charged with CuI (0.136 g, 0.716 mmol). The mixture in a sealed tube was heated at 130° C. overnight. After being cooled to room temperature, H2O and EtOAc were added. It was filtered through celite. The organic phase was separated, dried over Na2SO4, concentrated in vacuo. The residue was purified by a silica gel column, eluted with MeOH in CH2Cl2 (0-5% MeOH) to give (1-(3-fluoro-4-iodophenyl)-1H-imidazol-4-yl)methanol (0.39 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349873B2
Source datasetuspto-grants-2013_01
ORD IDord-2fe2ab17bf9e4d5c95ff2a1e5a7cddf7
Source noteuspto-grants-2013_01