Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Peracetic Acid | HCID 6585 | — |
| Reactant | HCID 70037884 | HCID 70037884 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 507294 | HCID 507294 | — |
Reaction Steps
Five grams [5.0 g (0.02 mole)] of 2-[[(5-Methyl-2-nitrophenyl) methyl]sulfinyl]pyridine-N-oxide, was slurried in 30 ml of glacial acetic acid. The slurry was stirred while 3.6 g of 40% peracetic acid (1.11 mole) was added dropwise. After addition, the mixture was heated to 60° C. for 4 hours, allowed to cool and stirred at room temperature overnight. Excess peracetic acid was destroyed using NaHSO3. The mixture was neutralized with K2CO3 solution, and the solid was filtered and washed with water. After drying, the solid melted at 178-183° C. and had an NMR consistent with the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06498254B1 |
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| Source dataset | uspto-grants-2002_12 |
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| ORD ID | ord-177e7a579ab346d080c7cb1ef3e9a4a1 |
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| Source note | uspto-grants-2002_12 |
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