HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 2-Methyl-3-hydroxy-4-acetyl-5-vinylpyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 2-Methyl-3-hydroxy-4-(1-hydroxyethyl)-5-vinylpyridine | HCID 20263921 | — |
| Catalyst | chromium (VI) trioxide | HCID 10219390 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Methyl-3-hydroxy-4-acetyl-5-vinylpyridine | HCID 20264046 | — |
Reaction Steps
To 750 ml. of dry methylene chloride containing 47.5 ml. of dry pyridine was added with stirring and cooling 29.6 g. of chromium trioxide. The mixture was aged 20 minutes at room temperature and then treated with a solution of 10.96 g. of the product from Example 10, Step B, in 250 ml. of dry methylene chloride over 15 minutes. After one hour at room temperature, the reaction mixture was filtered and the residue was washed with 2 × 100 ml. of methylene chloride. The methylene chloride filtrates were extracted with 3 × 500 ml. of 5% (w/w) aqueous sodium hydroxide solution, dried over magnesium sulfate and evaporated to dryness. The residue was crystallized from hexane to give 2-methyl-3-hydroxy-4-acetyl-5-vinylpyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04144342 |
| Source dataset | uspto-grants-1979_03 |
| ORD ID | ord-6409fe00a0df4a078faed1564a05d572 |
| Source note | uspto-grants-1979_03 |