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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228571Generated: October 25, 2026

Water → 2-[(6,7-Dimethoxy-4-quinolyl)oxy]-5-trifluoromethoxybenzaldehyde

https://huagongshe.com/reaction/228571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant4-Chloro-6,7-dimethoxyquinolineHCID 459610—
Reactant2-Hydroxy-5-(trifluoromethoxy)benzaldehydeHCID 1268058—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventChlorobenzeneHCID 7964—
Product2-[(6,7-Dimethoxy-4-quinolyl)oxy]-5-trifluoromethoxybenzaldehydeHCID 23078303—

Reaction Conditions

Temperature130 °C

Reaction Steps

4-Chloro-6,7-dimethoxyquinoline (111 mg), 5-trifluoromethoxysalicylaldehyde (412 mg), and 4-dimethylaminopyridine (244 mg) were suspended in monochlorobenzene (2 ml), and the suspension was stirred at 130° C. overnight. The reaction solution was cooled to room temperature, water was then added to the reaction solution, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was then washed with water and saturated brine and was dried over anhydrous sodium sulfate. The solvent was removed therefrom by distillation under the reduced pressure, and the residue was purified by chromatography on silica gel using ethyl acetate-hexane for development to give 2-[(6,7-dimethoxy-4-quinolyl)oxy]-5-trifluoromethoxybenzaldehyde.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560558B2
Source datasetuspto-grants-2009_07
ORD IDord-cd988899331d4b8587f8382755d24441
Source noteuspto-grants-2009_07