HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1096957Generated: October 25, 2026
Ethanol → Methyl 2-oxo-6-phenyl-1,2-dihydropyridine-4-carboxylate
https://huagongshe.com/reaction/1096957
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Methyl 2-(benzyloxy)-6-phenylisonicotinate | HCID 57930997 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl 2-oxo-6-phenyl-1,2-dihydropyridine-4-carboxylate | HCID 57931020 | — |
Reaction Steps
In a nitrogen atmosphere, 10% palladium-carbon (3.2 g) was added to an EtOH (50 mL)-THF (5 mL) mixed solution of methyl 2-phenyl-6-benzyloxypyridine-4-carboxylate (5.3 g), and in a hydrogen atmosphere, this was stirred at room temperature for 9 hours. The reaction liquid was filtered through Celite, concentrated under reduced pressure, and a mixed solution of hexane/ethyl acetate=2/1 was added thereto. The precipitate was taken out through filtration, washed with that solution, and dried to obtain the title compound as a white powder. The filtrate was concentrated, and the residue was purified through silica gel column chromatography (from hexane/ethyl acetate to chloroform/methanol), and combined with the previous powder to obtain the title compound as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08138197B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-63dba7c81586406ba9868bfb410f9916 |
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| Source note | uspto-grants-2012_03 |
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