HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → 1-(2-Hydroxyethyl)-1,2-dihydropyridin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | Ethyl 2-(2-oxopyridin-1-YL)acetate | HCID 9497629 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 1-(2-Hydroxyethyl)-1,2-dihydropyridin-2-one | HCID 253137 | 41.3% |
Reaction Steps
In 100 ml of dioxane, was dissolved N-ethoxycarbonylmethyl-2-pyridone (3.62 g, 20 mmol). To the solution was added 90% LiBH4 (0.96 g, 40 mmol) and the mixture was refluxed for 20 minutes. Subsequently, ethyl acetate (20 ml) was added to the mixture and the refluxing was carried out for five minutes. The reaction mixture was evaporated to dryness and water was added to the residue. The aqueous solution was extracted with chloroform (three times), dried, and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography, to thereby obtain the title compound (1.15 g, yield 41%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05935977 |
| Source dataset | uspto-grants-1999_08 |
| ORD ID | ord-749cdaefee5a47edb58d3ded2ec79fad |
| Source note | uspto-grants-1999_08 |