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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228581Generated: October 29, 2026

Water → {2-[(6,7-Dimethoxy-4-quinolyl)oxy]-5-methylphenyl}(2-furyl)methanone

https://huagongshe.com/reaction/228581

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-Furancarbonyl chlorideHCID 68242—
Reactant4-(2-Bromo-4-methylphenoxy)-6,7-dimethoxyquinolineHCID 23078362—
ReactantHCID 178418244HCID 178418244—
SolventTetrahydrofuranHCID 8028—
Product{2-[(6,7-Dimethoxy-4-quinolyl)oxy]-5-methylphenyl}(2-furyl)methanoneHCID 2487926633%

Reaction Conditions

Temperature-78 °C

Reaction Steps

4-(2-Bromo-4-methylphenoxy)-6,7-dimethoxyquinoline (100 mg) was dissolved in tetrahydrofuran (6 ml) to prepare a solution which was then cooled to −78° C. A 1.59 M n-butyllithium/hexane solution (0.35 ml) was added to the cooled solution, and the mixture was stirred at −78° C. for 20 min. 2-Furancarbonyl chloride (0.2 ml) was added to the reaction solution, and the mixture was stirred at room temperature for 7 hr. Further, water was 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 thin layer chromatography using acetone-chloroform to give the title compound (34 mg, yield 33%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560558B2
Source datasetuspto-grants-2009_07
ORD IDord-6e6e23cd8e494f818ab04a0fcdbeb9f7
Source noteuspto-grants-2009_07