HuagongsheHuagongshe Chemistry Print Report · For research reference only
Nitric Acid → 5-Methoxy-2-methyl-4-nitropyridine 1-oxide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 5-Methoxy-2-methyl-1-oxo-1lambda~5~-pyridine | HCID 12214019 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-Methoxy-2-methyl-4-nitropyridine 1-oxide | HCID 15163457 | — |
Reaction Steps
To fuming nitric acid (20 mL, Spectrochem, India) was added (5-methoxy-2-methylpyridine 1-oxide (14 g, 0.100 mol) in one lot and the reaction was stirred at rt for 2 h. Reaction progress was monitored by TLC (50% EtOAc in pet ether.). After completion of the reaction, the reaction mixture was poured in to ice water (100 mL) and neutralized with 40% NaOH solution (PH ˜7-7.5) to get a yellow precipitate. The precipitate was stirred for 5-10 min, then filtered and dried to give the title compound as a yellow solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 8.51 (s, 1H), 8.21 (s, 1H), 3.95 (s, 3H), 2.31 (s, 3H). MS (ESI, positive ion) m/z: 184.8 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08710043B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-ea0ec9f6da4c4ab8bb0d4cfc9c07687a |
| Source note | uspto-grants-2014_04 |