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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1023953Generated: November 2, 2026

Dichloromethane → 2-Fluoro-6-(5-fluoro-2-methoxy-4-vinylphenoxy)pyridine

https://huagongshe.com/reaction/1023953

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Ethenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 5233012—
Reactant2-(4-Bromo-5-fluoro-2-methoxyphenoxy)-6-fluoropyridineHCID 59191227—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product2-Fluoro-6-(5-fluoro-2-methoxy-4-vinylphenoxy)pyridineHCID 59191319—

Reaction Conditions

Temperature60 °C

Reaction Steps

To 2-(4-bromo-5-fluoro-2-methoxyphenoxy)-6-fluoropyridine (227 mg, 0.71 mmol) were added [1,1′-Bis(diphenylphosphino)ferrocene]dichloropalladium(II) complex with dichloromethane (58.9 mg, 0.07 mmol) and potassium carbonate (597 mg, 4.26 mmol). To the mixture were added acetonitrile (4 mL), water (1.3 mL) and vinyl boronic acid pinacol ester (180 μL, 1.07 mmol). The reaction was flushed with argon, and left to stir for 3 days at 60° C. The reaction mixture was then filtered on celite, rinsed with dichloromethane and concentrated. After purification by preparative TLC (cyclohexane/ethyl acetate: 70/30), the title product was isolated as an orange oil (166 mg, 89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722746B2
Source datasetuspto-grants-2014_05
ORD IDord-4813e6a6494d42f6a04d8cfda6e870fa
Source noteuspto-grants-2014_05