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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant6-Fluoronicotinic AcidHCID 242819—
SolventDimethylformamideHCID 6228—
ProductMethyl 6-fluoropyridine-3-carboxylateHCID 1375876584%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809342B2
Source datasetuspto-grants-2014_08
ORD IDord-8a16bd317de645bf8a628f3cb6722c91
Source noteuspto-grants-2014_08