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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228706Generated: October 30, 2026

4-Chloro-6,7-dimethoxyquinoline → HCID 57756484, compound

https://huagongshe.com/reaction/228706

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-6,7-dimethoxyquinolineHCID 459610—
Reactant1-(4-Chloro-2-hydroxyphenyl)ethanoneHCID 1051513—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
Solvent1,2-DichlorobenzeneHCID 7239—
ProductHCID 57756484HCID 5775648412%

Reaction Conditions

Temperature120 °C

Reaction Steps

4-Chloro-2-hydroxyacetophenone (45 mg), 4-chloro-6,7-dimethoxyquinoline (60 mg), and 4-dimethylaminopyridine (95 mg) are suspended in o-dichlorobenzene (10 ml) to prepare a suspension which was then stirred at 120° C. overnight and then at 140° C. for 5 hr. The reaction solution was cooled to room temperature, and the solvent was removed by distillation under the reduced pressure. Water was then added to the residue, and the mixture was extracted with chloroform. The chloroform layer was washed with water and was dried over anhydrous sodium sulfate, and the solvent was removed by distillation under the reduced pressure, and the residue was purified by thin layer chromatography using acetone-hexane to give the title compound (11 mg, yield 12%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560558B2
Source datasetuspto-grants-2009_07
ORD IDord-5e879dc3d08141aa9de7d4a9875e3262
Source noteuspto-grants-2009_07