Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228732Generated: October 30, 2026

4-Chloro-6,7-dimethoxyquinoline → HCID 23156477, compound

https://huagongshe.com/reaction/228732

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-6,7-dimethoxyquinolineHCID 459610—
Reactant1-(3-hydroxynaphthalen-2-yl)ethanoneHCID 598864—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
Solvent1,2-DichlorobenzeneHCID 7239—
ProductHCID 23156477HCID 2315647716.2%

Reaction Conditions

Temperature130 °C

Reaction Steps

1-(3-Hydroxynaphthalen-2-yl)-ethanone (249 mg), 4-chloro-6,7-dimethoxyquinoline (100 mg), and 4-(N,N-dimethylamino)-pyridine (164 mg) were dissolved in 1,2-dichlorobenzene (5 ml) to prepare a solution which was then stirred at 130° C. overnight. The reaction solution was cooled to room temperature, and the solvent was then removed by distillation under the reduced pressure. Water was added to the residue, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was then washed with water and was dried over anhydrous sodium sulfate. The solvent was removed by distillation under the reduced pressure. The residue was purified by thin layer chromatography using hexane-acetone to give the title compound (27 mg, yield 16%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560558B2
Source datasetuspto-grants-2009_07
ORD IDord-e3eebb54b347436eb987101c72ff4af2
Source noteuspto-grants-2009_07