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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220042Generated: October 30, 2026

Potassium Carbonate → Methyl 5-(4-(1,1-difluoroethyl)phenyl)nicotinate

https://huagongshe.com/reaction/220042

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantPotassium FluorideHCID 522689—
Reactant1-Bromo-4-(1,1-difluoroethyl)benzeneHCID 45158847—
Reactant[5-(Methoxycarbonyl)pyridin-3-yl]boronic acid hydrochlorideHCID 66890177—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductMethyl 5-(4-(1,1-difluoroethyl)phenyl)nicotinateHCID 58116582—

Reaction Steps

A solution of 2.98 g (13.3 mmol) of the compound from Example 48A in toluene (25.0 ml) was admixed under argon at RT with 3.62 g (16.7 mmol) of the compound from Example 33A in ethanol (8.4 ml) and 2.03 g (14.7 mmol) of potassium carbonate. After stirring for 10 min, 1.54 g (1.34 mmol) of tetrakis(triphenylphosphine)palladium and then 2.33 g (40.0 mmol) of potassium fluoride in water (5.8 ml) were added. The mixture was stirred under reflux for 8 h, and the reaction solution was cooled and diluted with ethyl acetate. The reaction solution was washed in water, and the organic phase was dried over magnesium sulphate, filtered and concentrated under reduced pressure. The residue was purified by means of column chromatography (silica gel, dichloromethane/methanol 100:1→80:1). Yield: 2.62 g (69% of theory, 4:1 mixture of methyl and ethyl ester)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202862B2
Source datasetuspto-grants-2012_06
ORD IDord-6a36d0dad148411fad4263377068b6fe
Source noteuspto-grants-2012_06