HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2406997Generated: October 31, 2026
Methyl iodide → Methyl 6-fluoropyridine-3-carboxylate
https://huagongshe.com/reaction/2406997
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 6-Fluoronicotinic Acid | HCID 242819 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 6-fluoropyridine-3-carboxylate | HCID 13758765 | 84% |
Reaction Steps
A round bottom flask was charged with K2CO3 (191 g, 1380 mmol), 6-fluoronicotinic acid (77.8 g, 551 mmol) and dimethylformamide (551 mL). Methyl iodide (51.5 mL, 827 mmol) was then added in one portion at room temperature and mixture stirred overnight at room temperature. The reaction mixture was partitioned between ethyl acetate and water. The organic layer was washed three times with water and once with brine, and then dried over Na2SO4. Purification by silica gel flash chromatography (ethyl acetate/dichloromethane) gave 6-fluoro-nicotinic acid methyl ester (71.8 g, 84%) as a white solid. 1H NMR (400 MHz, CDCl3, δ): 3.96 (s, 3 H) 7.01 (dd, J=8.58, 2.93 Hz, 1 H) 8.41 (ddd, J=8.49, 7.61, 2.44 Hz, 1 H) 8.89 (d, J=2.34 Hz, 1 H); MS (M+1): 156.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08809342B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-8a16bd317de645bf8a628f3cb6722c91 |
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| Source note | uspto-grants-2014_08 |
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