Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454135Generated: October 31, 2026

Sodium Hydroxide → 3-Fluoro-7-methoxy-2-methylquinoline

https://huagongshe.com/reaction/454135

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantAmmonium ChlorideHCID 25517—
Reactant2-Chloro-3-fluoro-7-methoxyquinolineHCID 22030591—
ReactantHCID 178418573HCID 178418573—
Catalystcopper(I) bromideHCID 24593—
SolventTetrahydrofuranHCID 8028—
Product3-Fluoro-7-methoxy-2-methylquinolineHCID 2203079291%

Reaction Conditions

Temperature-78 °C

Reaction Steps

2-Chloro-3-fluoro-7-methoxyquinoline (210 g, 1 mmol), (prepared as described for the starting material in Example 157), in anhydrous THF (1 ml) was added to a mixture of copper(I)bromide (570 mg, 4.0 mmol) and methylmagnesium bromide (3.0M solution in diethyl ether, 2.7 ml, 8 mmol) in anhydrous THF (20 ml) at −78° C. The mixture was stirred for 1 hour at −78° C., allowed to warm to ambient temperature and then stirred for a further 18 hours. Saturated aqueous ammonium chloride solution and 5N aqueous sodium hydroxide solution (pH 12) were added and the product extracted with ethyl acetate (3×). The organic solution was washed with water, brine, dried (MgSO4) and evaporated to dryness to yield 3-fluoro-7-methoxy-2-methylquinoline (0.17 g, 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492560B2
Source datasetuspto-grants-2013_07
ORD IDord-ed7068db105d4f9788a278b38ebf3778
Source noteuspto-grants-2013_07