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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228625Generated: October 25, 2026

4-Chloro-6,7-dimethoxyquinoline → HCID 57756350, compound

https://huagongshe.com/reaction/228625

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-6,7-dimethoxyquinolineHCID 459610—
ReactantEthyl 2-hydroxy-6-methylbenzoateHCID 584222—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
Solvent1,2-DichlorobenzeneHCID 7239—
ProductHCID 57756350HCID 5775635091.3%

Reaction Conditions

Temperature120 °C

Reaction Steps

4-Chloro-6,7-dimethoxyquinoline (112 mg), ethyl 6-methylsalicylate (360 mg), and 4-dimethylaminopyridine (244 mg) were suspended in o-dichlorobenzene (1 ml), and the suspension was stirred at 120° C. overnight and was further stirred at 140° C. for 2 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. The solvent was removed therefrom by distillation under the reduced pressure, and the residue was purified by column chromatography using acetone-hexane to give the title compound (168 mg, yield 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560558B2
Source datasetuspto-grants-2009_07
ORD IDord-9845176dbbe1460683bc8cdfa08873e6
Source noteuspto-grants-2009_07