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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-(Trifluoromethyl)pyridine-3-carbonitrile | HCID 2736743 | — |
| Solvent | Ethylene Glycol | HCID 174 | — |
| Product | 3-Pyridinecarboxylic acid, 4-(trifluoromethyl)- | HCID 2777549 | 84% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07015236B2 |
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| Source dataset | uspto-grants-2006_03 |
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| ORD ID | ord-2ae3ab0f362642ed9142bf19a7bc83a6 |
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| Source note | uspto-grants-2006_03 |
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