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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1744279Generated: November 1, 2026

Hydrochloric Acid → 3-Pyridinecarboxylic acid, 4-(trifluoromethyl)-

https://huagongshe.com/reaction/1744279

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantPotassium HydroxideHCID 14797—
Reactant4-(Trifluoromethyl)pyridine-3-carbonitrileHCID 2736743—
SolventEthylene GlycolHCID 174—
Product3-Pyridinecarboxylic acid, 4-(trifluoromethyl)-HCID 277754984%

Reaction Conditions

Temperature20 °C

Reaction Steps

3-Cyano-4-trifluoromethylpyridine (11.47 g, 66.64 mmol) was suspended in ethylene glycol (76 ml) and 85% potassium hydroxide (13.20 g, 200 mol) was added. The mixture was stirred under heating at 20° C. for 4 hours. The reaction solution was cooled to room temperature and then water (50 ml) and 4N hydrochloric acid (60 ml) were added. The resulting reaction mixture was extracted with ethyl acetate four times. The organic layers were combined, washed with saturated salt water, dried over magnesium sulfate, and then concentrated under reduced pressure to obtain 10.70 g (yield 84.0%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07015236B2
Source datasetuspto-grants-2006_03
ORD IDord-2ae3ab0f362642ed9142bf19a7bc83a6
Source noteuspto-grants-2006_03