HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 2,3,5-Trimethyl-1-oxidopyridin-1-ium
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2,3,5-Trimethylpyridine | HCID 12759 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2,3,5-Trimethyl-1-oxidopyridin-1-ium | HCID 10486907 | 94.5% |
Reaction Steps
To acetic acid (1.43 kg, 23.83 mol), 2,3,5-trimethylpyridine (1.43 kg, 11.80 mol) was added over 15 minutes. After 15 minutes, a 35% hydrogen peroxide solution (1.38 kg, 14.2 mol) was added dropwise over 30 minutes, the mixture was stirred at 90° C. to 95° C. overnight. To the reaction mixture, sodium sulfite (220 g) was added. The reaction mixture was poured into a mixture of sodium carbonate (2.5 kg) and water (12 L) and the mixture was extracted with chloroform (3.0 L×4). The organic layer obtained was concentrated until crystal precipitated. To the precipitate, n-hexane (2.5 L) was added. The resultant mixture was stirred under ice-cool overnight The resultant solid was filtrated to obtain a desired compound (1.53 kg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07425634B2 |
| Source dataset | uspto-grants-2008_09 |
| ORD ID | ord-835a3f9320ec4f6fbf1a220927959d79 |
| Source note | uspto-grants-2008_09 |