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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228576Generated: October 26, 2026

Water → 1-{2-[(6,7-Dimethoxy-4-quinolyl)oxy]-5-methylphenyl}-3,3-dimethyl-1-butanone

https://huagongshe.com/reaction/228576

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant3,3-Dimethylbutanoyl chlorideHCID 81514—
Reactant4-(2-Bromo-4-methylphenoxy)-6,7-dimethoxyquinolineHCID 23078362—
ReactantHCID 178418244HCID 178418244—
SolventTetrahydrofuranHCID 8028—
Product1-{2-[(6,7-Dimethoxy-4-quinolyl)oxy]-5-methylphenyl}-3,3-dimethyl-1-butanoneHCID 5775657314%

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 (0.4 ml) was added thereto, and the mixture was stirred at −78° C. for 20 min. Tert-butylacetyl chloride (0.2 ml) was added to the reaction solution, and the mixture was stirred at room temperature overnight. 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 (15 mg, yield 14%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560558B2
Source datasetuspto-grants-2009_07
ORD IDord-b98517eee7954c81ad0061772a533b7f
Source noteuspto-grants-2009_07