HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 878231Generated: October 30, 2026
Hydrochloric Acid → HCID 70663168, compound
https://huagongshe.com/reaction/878231
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 2-Chloro-6-(trifluoromethyl)pyridine-4-carboxylic acid | HCID 11218389 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 70663168 | HCID 70663168 | 90.4% |
Reaction Steps
To a solution of 2-chloro-6-(trifluoromethyl)isonicotinic acid (0.15 g, 665 μmol, prepared according to F. Cottet, M. Schlosser, Eur. J. Org. Chem. 2004, 18, 3793-3798) in methanol (2 mL) sodium methoxide (79.0 mg, 1.46 mmol) was added and the reaction refluxed for 5 hours. Another 287 mg (5.32 mmol) sodium methoxide was added and the white suspension was stirred at reflux temperature overnight. After 23 hours the suspension was allowed to cool to room temperature and was poured on saturated 1M HCl solution and EtOAc and the layers were separated. The aqueous layer was extracted twice with EtOAc. The organic layers were washed once with brine, dried over MgSO4, filtered and evaporated to give the desired compound as a colorless solid (0.133 g; 90%). MS (ESI): m/z=220.02 [M−H]−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08987307B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-4c621cb4f9d342bbb64dbda2aa5e085a |
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| Source note | uspto-grants-2015_03 |
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