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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1963196Generated: October 26, 2026

Potassium Carbonate → Methyl 2-(3,4,5-trifluorophenyl)isonicotinate

https://huagongshe.com/reaction/1963196

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(3,4,5-Trifluorophenyl)boronic Acid (contains varying amounts of Anhydride)HCID 2734671—
Reactant2-Bromo-isonicotinic acid methyl esterHCID 3847768—
CatalystPalladium ChlorideHCID 24290—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductMethyl 2-(3,4,5-trifluorophenyl)isonicotinateHCID 6673230852.9%

Reaction Conditions

Temperature100 °C

Reaction Steps

Methyl 2-bromoisonicotinate (4 g, 18.52 mmol), 3,4,5-trifluorophenylboronic acid (4.89 g, 27.77 mmol), potassium carbonate (3.84 g, 27.77 mmol) and PdCl2 (dppf) (0.402 g, 0.56 mmol) were mixed in methanol (30 mL) in two separate 20 mL microwave vials. The vials were capped and heated at 100° C. for 10 min in a single node microwave reactor. Water and DCM were added and the phases were separated. The water phase (pH 9) was extracted with DCM and the combined organic phase washed with brine, passed through a phase separator and evaporated to yield a brown solid. The residue was dissolved in DCM and purified by SCX-2 cation exchange chromatography. Methyl 2-(3,4,5-trifluorophenyl)isonicotinate (2.62 g, 52%) was isolated as a slightly yellow solid. MS m/z 268 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415378B2
Source datasetuspto-grants-2013_04
ORD IDord-5c8f2e49c53b41fd866ec5ae6c644456
Source noteuspto-grants-2013_04