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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1963219Generated: October 30, 2026

Hydrochloric Acid → Methyl 2-(2-fluoro-4-(trifluoromethyl)phenyl)isonicotinate hydrochloride

https://huagongshe.com/reaction/1963219

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 2-chloropyridine-4-carboxylateHCID 2736842—
Reactant2-Fluoro-4-(trifluoromethyl)benzeneboronic acidHCID 16414145—
CatalystPalladium ChlorideHCID 24290—
SolventMethanolHCID 887—
Solventtert-Butyl methyl etherHCID 15413—
ProductMethyl 2-(2-fluoro-4-(trifluoromethyl)phenyl)isonicotinate hydrochlorideHCID 6673233899%

Reaction Conditions

Temperature100 °C

Reaction Steps

Methyl 2-chloroisonicotinate (2.8 g, 16.32 mmol), 2-fluoro-4-(trifluoromethyl)phenylboronic acid (5.09 g, 24.48 mmol), potassium carbonate (1.692 g, 12.24 mmol) and PdCl2 (dppf) (0.354 g, 0.49 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 dark-orange solid. The solid was dissolved in MTBE and stirred for 15 minutes, then filtered. The orange MTBE layer was treated with hydrogen chloride (4 M in dioxane, 4.08 mL, 16.32 mmol) and stirred for 1 h at room temperature. The precipitate was collected by filtration. Methyl 2-(2-fluoro-4-(trifluoromethyl)phenyl)isonicotinate hydrochloride (5.4 g, 99%) was isolated as a slightly orange solid. MS m/z 300 (M+H)+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08415378B2
Source datasetuspto-grants-2013_04
ORD IDord-766f86eed66f479ea83c4d4c0eb803be
Source noteuspto-grants-2013_04