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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337539Generated: October 29, 2026

Anisole → Methyl 6-oxo-1,6-dihydropyridine-3-carboxylate

https://huagongshe.com/reaction/337539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnisoleHCID 7519—
ReactantMethyl 6-(4-methoxybenzyloxy)nicotinateHCID 23144104—
SolventTrifluoroacetic acidHCID 6422—
ProductMethyl 6-oxo-1,6-dihydropyridine-3-carboxylateHCID 41634389.3%

Reaction Steps

Methyl 6-(4-methoxybenzyloxy)nicotinate (2.66 g, 9.73 mmol) obtained in Step 2 and anisole (10.6 mL) were dissolved in trifluoroacetic acid (15 mL), followed by stirring at room temperature for 30 minutes. The reaction mixture was concentrated under reduced pressure, and saturated sodium hydrogencarbonate was added to the resulting residue, followed by extraction with chloroform. The organic layer was dried over anhydrous magnesium sulfate, and then the solvent was distilled away under reduced pressure. The precipitated solid was collected by filtration to afford methyl 2-oxo-1,2-dihydropyridine-5-carboxylate (1.33 g, 89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889718B2
Source datasetuspto-grants-2014_11
ORD IDord-58d15164297c4b9f9c7a1a40758478d9
Source noteuspto-grants-2014_11