HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 398252Generated: October 25, 2026
Acetic Acid → 3-Methoxy-2-methylpyridine 1-oxide
https://huagongshe.com/reaction/398252
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Potassium Bromide | HCID 253877 | — |
| Reactant | 3-Methoxy-2-methylpyridine | HCID 3015270 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Methoxy-2-methylpyridine 1-oxide | HCID 12214016 | 16.7% |
Reaction Steps
To a solution obtained by dissolving 3-methoxy-2-methylpyridine (14.8 g, 0.12 mol) in acetic acid (44 g, 0.12×2.5 mol) was added 31% hydrogen peroxide (33 g, 0.12×2.5 mol), followed by stirring in an oil bath at 100° C. for 16 hours. The reaction solution was then cooled and poured into iced-water. To the mixture was then added sodium carbonate (solid) so as to be weak alkalinity. The resultant solution was extracted with ethyl acetate to obtain 1.45 g (percent yield: 16.7%) of 3-methoxy-2-methylpyridine-N-oxide IR KBr cm−1: 1668, 1647, 1584, 1503, 1302, 1266, 1188, 1128, 792. 1H-NMR (60 MHz, CDCl3, δ): 2.4 (3R, s, CH3), 3.8 (3H, s, OCH3), 6.5-7.2 (2H, m, pyridine ring H×2), 7.7-8.0 (1H, m, pyridine ring H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06610853B1 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-dde7fcb5f8cf429d9beeef8755c09d37 |
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| Source note | uspto-grants-2003_08 |
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