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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2291109Generated: November 1, 2026

Hydrogen Peroxide → 2,3,5-Trimethyl-1-oxidopyridin-1-ium

https://huagongshe.com/reaction/2291109

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
Reactant2,3,5-TrimethylpyridineHCID 12759—
SolventAcetic AcidHCID 176—
Product2,3,5-Trimethyl-1-oxidopyridin-1-iumHCID 10486907243.6%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a 100 liters reaction vessel was added 2,3,5-trimethyl-pyridine (10.9 kg, 89.2 moles) and acetic acid (30 liters). The temperature was raised to 90° C. The mixture was stirred for 3 hours and thereafter cooled to 60° C., whereafter H2O2 (35% solution, 3122 ml, 35.67 moles) was added during 1 hour. The temperature was then raised to 90° C. The reaction mixture was stirred overnight. After cooling to 40° C. an additional amount of H2O2 solution (936 ml, 10.7 moles) was added during 1 hour. The temperature was then raised to 90° C. The reaction mixture was stirred for 3 hours and was allowed to stand without heating overnight. Excess of acetic acid was distilled off under vaccum. To the remainder was added NaOH (10M) until pH 10. CH2Cl2 (10 liters) was added and the resulting mixture was stirred vigorously. The CH2Cl2 phase was separated and the water phase was extracted twice with CH2Cl2 (10 liters). The combined CH2Cl2 -phases were dried over MgSO4 and filtrated. The filtrate was evaporated yielding 2,3,5-trimethyl-pyridine-N-oxide (11920 g, 94% purity). The identity of the product was confirmed with 1H and 13C NMR.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04620008
Source datasetuspto-grants-1986_10
ORD IDord-5dfc6b339ef04ccfa6b2cd97d307d11f
Source noteuspto-grants-1986_10