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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2178342Generated: October 29, 2026

Potassium Carbonate → 5-((4-Bromo-5-fluoro-2-methoxyphenoxy)methyl)-2-methoxypyridine

https://huagongshe.com/reaction/2178342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Bromo-5-fluoro-2-methoxyphenolHCID 26596525—
Reactant5-(Chloromethyl)-2-methoxypyridine hydrochlorideHCID 53438957—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product5-((4-Bromo-5-fluoro-2-methoxyphenoxy)methyl)-2-methoxypyridineHCID 11811398066%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a stirred solution of 4-bromo-5-fluoro-2-methoxyphenol (2.82 g, 12.25 mmol) in N,N-dimethylformamide (50 mL) was added 5-(chloromethyl)-2-methoxypyridine hydrochloride (2.50 g, 12.86 mmol) and potassium carbonate (5.08 g, 36.75 mmol). The reaction mixture was heated to 100° C. After 2 h, the mixture was allowed to cool to room temperature and was diluted with water. The mixture was extracted with ethyl acetate (3×25 mL). The combined organic phases were washed with brine, dried over magnesium sulfate, filtered, and concentrated. Chromatographic purification (0-33% ethyl acetate/hexanes elute) afforded 2.76 g (66%) of 5-((4-bromo-5-fluoro-2-methoxyphenoxy)methyl)-2-methoxypyridine as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067914B1
Source datasetuspto-grants-2015_06
ORD IDord-84e4e516a7644a02ad5e2b2925c62aeb
Source noteuspto-grants-2015_06