Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 2,3-Lutidine | HCID 11420 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Sulfuric Acid | HCID 1118 | — |
| Product | Pyridine, 2,3-dimethyl-, 1-oxide | HCID 3840573 | — |
Reaction Steps
One hundred g. of 2,3-lutidine was dissolved into 200 ml. of glacial acetic acid, followed by dropwise addition of 120 g. of 35% aqueous hydrogen peroxide solution at about 40° C. The mixture was allowed to react at 105° C. for about 2 hours. After completion of the reaction, the mixture was cooled down to about 50° C., followed by addition of 5.0 g. of p-formaldehyde. The resultant mixture was heated to 105° C. to cause the reaction to take place for about 10 minutes. The resultant mixture was cooled down to about 40° C., followed by addition of 150 g. of 98% sulfuric acid. The resultant mixture was subjected to distillation under reduced pressure to evaporate the glacial acetic acid off to give 2,3-dimethylpyridine N-oxide as a sulfuric acid solution.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06002011 |
|---|
| Source dataset | uspto-grants-1999_12 |
|---|
| ORD ID | ord-128f62199c0246bf873dffbfc77ad853 |
|---|
| Source note | uspto-grants-1999_12 |
|---|