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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1967868Generated: November 2, 2026

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

https://huagongshe.com/reaction/1967868

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 numberUS08420827B2
Source datasetuspto-grants-2013_04
ORD IDord-c3515f9f693443cf80d621871cf7da0e
Source noteuspto-grants-2013_04