HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2231954Generated: October 27, 2026
Hydrogen Peroxide → 4-Methoxy-2,3,5-trimethylpyridine 1-oxide
https://huagongshe.com/reaction/2231954
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | 4-Methoxy-2,3,5-trimethylpyridine | HCID 127899 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 4-Methoxy-2,3,5-trimethylpyridine 1-oxide | HCID 10702237 | — |
Reaction Steps
100 g 4-methoxy-2,3,5-trimethylpyridine was dissolved in 300 ml glacial acetic acid and 100 ml 50% hydrogenperoxide and stirred at 30° C. for 1 h. The temperature was gradually heated to70° C. and was maintained for 5 hrs and the temperature increased to 90° C. and a small amount of Pd/C added to destroy excess hydrogenperoxide. After testing that the peroxide was destroyed the solvents were evaporated at reduced pressure. Toluene was added and stripped off to make the product free from water. After the product was dry most of the toluene was evaporated in vacuum. The 4-methoxy-2,3,5-trimethylpyridine N-oxide was diluted with acetic acid and used directly in the next step. The yield of N-oxide was 95%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04785113 |
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| Source dataset | uspto-grants-1988_11 |
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| ORD ID | ord-4007545b6ec0477990b7676aa0035216 |
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| Source note | uspto-grants-1988_11 |
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