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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrogen PeroxideHCID 784—
ReactantSodium CarbonateHCID 10340—
ReactantPotassium BromideHCID 253877—
Reactant3-Methoxy-2-methylpyridineHCID 3015270—
SolventWaterHCID 962—
Product3-Methoxy-2-methylpyridine 1-oxideHCID 1221401616.7%

Reaction Conditions

Temperature100 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610853B1
Source datasetuspto-grants-2003_08
ORD IDord-dde7fcb5f8cf429d9beeef8755c09d37
Source noteuspto-grants-2003_08