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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339042Generated: October 25, 2026

Water → 8-(Difluoromethoxy)-6-fluoro-2-methylquinoline

https://huagongshe.com/reaction/339042

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAcetonitrileHCID 6342—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-2,2-difluoroacetophenoneHCID 238296—
Reactant6-Fluoro-8-hydroxy-2-methylquinolineHCID 66781517—
Product8-(Difluoromethoxy)-6-fluoro-2-methylquinolineHCID 70984374—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a mixture of 6-fluoro-2-methylquinolin-8-ol (0.15 g, 0.85 mmol) and potassium carbonate (4.2 g, 30 mmol) in acetonitrile (3.4 mL, 0.85 mmol) and water (3.4 mL, 0.85 mmol) was added 2-chloro-2,2-difluoroacetophenone (0.62 mL, 4.2 mmol). The vessel was sealed and the mixture was heated at 80° C. for 4 hours. The cooled reaction mixture was extracted with diethyl ether (2×30 mL), and the combined organic extracts were dried over magnesium sulfate, filtered and concentrated under reduced pressure at ambient temperature The resulting residue was purified by reverse phase chromatography on a C18 column (0-100% acetonitrile/water). Aqueous fractions containing the product were combined and extracted with diethyl ether (2×100 mL). The combined organic extracts were dried over magnesium sulfate, filtered and concentrated under reduced pressure at ambient temperature providing the title compound. Presence of water was noted and the material taken on as is assuming theoretical yield obtained (0.19 g, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889704B2
Source datasetuspto-grants-2014_11
ORD IDord-75c94b7ae1fc4b6fba7882526e3a2fab
Source noteuspto-grants-2014_11