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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 228528Generated: October 27, 2026

Water → 4-[(6-Bromo-2-naphthyl)oxy]-6,7-dimethoxyquinoline

https://huagongshe.com/reaction/228528

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAcetyl chlorideHCID 6367—
Reactant4-[(1,6-Dibromo-2-naphthyl)oxy]-6,7-dimethoxyquinolineHCID 68829718—
ReactantHCID 178418244HCID 178418244—
SolventTetrahydrofuranHCID 8028—
Product4-[(6-Bromo-2-naphthyl)oxy]-6,7-dimethoxyquinolineHCID 5775632651.4%

Reaction Conditions

Temperature-78 °C

Reaction Steps

4-[(1,6-Dibromo-2-naphthyl)oxy]-6,7-dimethoxyquinoline (65 mg) was dissolved in tetrahydrofuran (3 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. Acetyl 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 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 (28 mg, yield 51%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560558B2
Source datasetuspto-grants-2009_07
ORD IDord-2543c3d4a98242d88cc0c7131bc94f2e
Source noteuspto-grants-2009_07