Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2,3-Lutidine | HCID 11420 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Hydrogen Peroxide | HCID 784 | — |
| Product | Pyridine, 2,3-dimethyl-, 1-oxide | HCID 3840573 | — |
Reaction Steps
71.79 g of 2,3-dimethylpyridine (II) was dissolved in 240 ml of acetic acid, to which 40 ml of 30% hydrogen peroxide solution was added and the resulting mixture was heated at 95° C. for 3 hours. Furthermore, 18 ml of a 30% hydrogen peroxide solution was added to the mixture and heated at 95° C. for 13 hours, and thereafter, 700 ml of water was added thereto and the resulting mixture was neutralized with sodium carbonate and extracted with chloroform. The resulting organic layer was dried over anhydrous sodium sulfate and the solvent was distilled off under reduced pressure. The resulting precipitation was recrystallized from diisopropylether to obtain 71.34 g of 2,3-dimethylpyridine N-oxide (III).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06525066B2 |
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| Source dataset | uspto-grants-2003_02 |
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| ORD ID | ord-5db019416a4342aa958ad1ddfeb901d1 |
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| Source note | uspto-grants-2003_02 |
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