HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1501206Generated: November 3, 2026
Methanol → (R)-2-oxo-1-(1-phenylethyl)-1,2-dihydropyridine-4-carboxylic acid
https://huagongshe.com/reaction/1501206
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Lithium hydroxide, monohydrate | HCID 168937 | — |
| Reactant | (R)-methyl 2-oxo-1-(1-phenylethyl)-1,2-dihydropyridine-4-carboxylate | HCID 89585124 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (R)-2-oxo-1-(1-phenylethyl)-1,2-dihydropyridine-4-carboxylic acid | HCID 89585123 | 80% |
Reaction Steps
A mixture of (R)-methyl 2-oxo-1-(1-phenylethyl)-1,2-dihydropyridine-4-carboxylate (451 mg, 1.75 mmol), lithium hydroxide monohydrate (369 mg, 8.77 mmol), water (4 mL) and methanol (4 mL) in tetrahydrofuran (12 mL) was stirred at 20° C. for 12 hours. The reaction mixture was concentrated. The residue was acidified with concentrated hydrochloride solution to pH=2. The mixture was extracted with ethyl acetate (20 mL×2). The organic phase was dried over sodium sulfate and filtered. The filtrate was concentrated. The residue was purified by column chromatography (silica gel, petroleum ether/ethyl acetate=1:2) to give (R)-2-oxo-1-(1-phenylethyl)-1,2-dihydropyridine-4-carboxylic acid as a white solid (336 mg, 80%). LRMS (M+H+) m/z: calcd 243.13. found 243.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09206128B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-3d6f95ffdd4345649371b01fb030891b |
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| Source note | uspto-grants-2015_12 |
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