HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172122Generated: October 26, 2026
Water → Methyl 4-(trifluoromethyl)nicotinate
https://huagongshe.com/reaction/1172122
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Pyridinecarboxylic acid, 4-(trifluoromethyl)- | HCID 2777549 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 4-(trifluoromethyl)nicotinate | HCID 2775680 | 56.1% |
Reaction Steps
6.7 g (48.6 mmoles) of anhydrous potassium carbonate and 6.9 g (48.6 mmoles) of methyl iodide were added to a solution of 4.6 g (24.1 mmoles) of 4-trifluoromethylnicotinic acid dissolved in 70 ml of N,N-dimethylformamide. The mixture was stirred at room temperature for 12 hours to give rise to a reaction. After confirmation of the completion of the reaction, the reaction mixture was poured into water, followed by extraction with ethyl acetate. The resulting organic layer was washed with water and an aqueous sodium chloride solution and then dried over anhydrous magnesium sulfate. The resulting solution was subjected to vacuum distillation to remove the solvent contained therein. The residue was purified by silica gel column chromatography (developing solvent: hexane-ethyl acetate mixed solvent) to obtain 2.77 g (yield: 56.1%) of methyl 4-trifluoromethylnicotinate as a yellow oily substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07833939B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-c34d097382a1481a9be250c51b2aaae4 |
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| Source note | uspto-grants-2010_11 |
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