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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1802621Generated: October 29, 2026

8-Hydroxyquinoline → HCID 18453089, compound

https://huagongshe.com/reaction/1802621

Reaction equation

Participants

RoleNameHCIDCharge
Reactant8-HydroxyquinolineHCID 1923—
ReactantPotassium CarbonateHCID 11430—
Reactantp-DiiodobenzeneHCID 12208—
ReactantHCID 178516071HCID 178516071—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductHCID 18453089HCID 1845308936.2%

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of 1,4-diiodobenzene 1-1 (4.00 g, 12.1 mmol), 2-hydroxypyridine 1-7 (1.15 g, 12.1 mmol), 8-hydroxyquinoline (176 mg, 1.21 mmol) and K2CO3 (1.74 g, 12.6 mmol) in DMSO (16 mL) was degassed with Ar before being charged with CuI (230 mg, 1.21 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 EtOAc in hexanes (0-70% EtOAc) to give 1-(4-iodophenyl)pyridin-2(1H)-one (1.30 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349873B2
Source datasetuspto-grants-2013_01
ORD IDord-b287a01d452b4558b15ac954f23d98c1
Source noteuspto-grants-2013_01