HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 4-Pyridinone,3-OH-2-Me
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | 3-(BENZYLOXY)-2-METHYL-4(1H)-PYRIDINONE | HCID 2726416 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Glycerol | HCID 753 | — |
| Product | 4-Pyridinone,3-OH-2-Me | HCID 323814 | 71% |
Reaction Steps
4.2 g (14.5 mmol) of 2-methyl-3-benzyloxypyridine-4(1H)-one of glycerol is put into the mixture of 54 mL ethanol—6 mL H2O, and 0.11 g of Pd/C at 10% is added. The reaction medium is subjected to catalytic hydrogenolysis under agitation at room temperature for 24 hours. At the end of this hydrogenolysis, the reaction medium is filtered. The filtered Pd/C is washed with EtOH; then the filtrate is evaporated under reduced pressure. The solid residue is re-crystallized in a MeOH-ethyl acetate mixture to obtain 2.05 g (10.3 mmol) of 2-methyl-3-hydroxypyridine-4(1H)-one of glycerol, which is pure at chromatographic and NMR analyses. Yield: 71%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06177409B1 |
| Source dataset | uspto-grants-2001_01 |
| ORD ID | ord-2d9813b6a75a4236958be0b7c47b6c44 |
| Source note | uspto-grants-2001_01 |