HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 4-(Hydroxymethyl)pyridin-2(1H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Methyl 2-oxo-1,2-dihydropyridine-4-carboxylate | HCID 280755 | — |
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Chloroform methanol | HCID 21584188 | — |
| Product | 4-(Hydroxymethyl)pyridin-2(1H)-one | HCID 11094610 | — |
Reaction Steps
2-Oxo-1,2-dihydropyridine-4-carboxylic acid methyl ester (1.8 g, 12.2 mmol), prepared as described in J. Org. Chem., 26, 428 (1961), was suspended in THF(100 ml). A small amount of DMF was added to help increase solubility. LiBH4 (61 mmol) was added and the reaction was stirred for 18 hours at room temperature. MeOH and H2O are added to quench the reaction. The reaction is then concentrated to yield a yellow oil. Flash chromatography (5% MeOH/CHCl3 to 20% MeOH/CHCl3) yielded 4-hydroxymethyl-1H-pyridin-2-one as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06093737 |
| Source dataset | uspto-grants-2000_07 |
| ORD ID | ord-24944cd9dfbb4e2a8c8636f53f6911d9 |
| Source note | uspto-grants-2000_07 |