HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 1-Acetyl-3-(benzyloxy)-2-methylpyridin-4(1H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Acetyl bromide | HCID 10482 | — |
| Reactant | 2-Methyl-3-(phenylmethoxy)-4(3H)-pyridinone | HCID 69343794 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 1-Acetyl-3-(benzyloxy)-2-methylpyridin-4(1H)-one | HCID 18688776 | 64.8% |
Reaction Steps
1 3-Benzyloxy-2-methylpyrid-4-one (4 g) is dissolved in dry acetone (100 ml). Acetylbromide (3 g) and triethylamine (2.7 g) are added and the resulting mixture is mechanically stirred overnight. The mixture is then filtered and the filtrate is rotary evaporated to dryness. The residue is dissolved in methylene chloride and washed with dilute hydrochloric acid (pH 3.0), then twice with water, and is dried over Na2SO4 and rotary evaporated to yield a solid residue. Recrystallisation of this residue from an ethylacetate/hexane mixture gives 1-acetyl-3-benzyloxy-2-methylpyrid-4-one as an oil (3.1 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | USRE035948 |
| Source dataset | uspto-grants-1998_11 |
| ORD ID | ord-a037f7bcfe7c47cf8468dd12e62eb72f |
| Source note | uspto-grants-1998_11 |