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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 661247Generated: November 2, 2026

Potassium Carbonate → Methyl 5-[3-fluoro-4-(2,2,2-trifluoroethyl)phenyl]nicotinate

https://huagongshe.com/reaction/661247

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantPotassium FluorideHCID 522689—
Reactant4-Bromo-2-fluoro-1-(2,2,2-trifluoroethyl)benzeneHCID 54310924—
Reactant[5-(Methoxycarbonyl)pyridin-3-yl]boronic acid hydrochlorideHCID 66890177—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductMethyl 5-[3-fluoro-4-(2,2,2-trifluoroethyl)phenyl]nicotinateHCID 58116533—

Reaction Steps

A solution of 6.78 g (23.7 mmol, purity 90%) of the compound from Example 74A in toluene (339 ml) was admixed under argon at RT with 7.74 g (35.6 mmol) of the compound from Example 29A in ethanol (112 ml) and 3.61 g (26.1 mmol) of potassium carbonate. After stirring for 10 min, 2.74 g (2.37 mmol) of tetrakis(triphenylphosphine)palladium and then 4.14 g (71.2 mmol) of potassium fluoride in water (71 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, dichloromethane/methanol 150:1→100:1). The product fractions were concentrated under reduced pressure and the solid obtained was purified by stirring with diethyl ether. Yield: 6.00 g (50% of theory, purity 62%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08084469B2
Source datasetuspto-grants-2011_12
ORD IDord-0f85fc2012e24b76bfc6449bd39a0e12
Source noteuspto-grants-2011_12