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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228873Generated: October 30, 2026

1,2-Dichlorobenzene → HCID 23078374, compound

https://huagongshe.com/reaction/228873

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichlorobenzeneHCID 7239—
Reactant4-Chloro-6,7-dimethoxyquinolineHCID 459610—
ReactantHCID 23078302HCID 23078302—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
ProductHCID 23078374HCID 2307837412%

Reaction Conditions

Temperature120 °C

Reaction Steps

6-Hydroxy-5-iodo-quinoline (100 mg), 4-chloro-6,7-dimethoxyquinoline (215 mg), and 4-dimethylaminopyridine (367 mg) were suspended in o-dichlorobenzene (12 ml), and the suspension was stirred at 120° 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 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, and the residue was purified by thin layer chromatography using acetone-chloroform to give the title compound (20 mg, yield 12%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560558B2
Source datasetuspto-grants-2009_07
ORD IDord-296d633d444b4a2aa49373fc397fe381
Source noteuspto-grants-2009_07