HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 250939Generated: October 30, 2026
Hydrogen Peroxide → 3-Isopropyl-2-methyl-1-oxidopyridin-1-ium
https://huagongshe.com/reaction/250939
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | 2-Methyl-3-(propan-2-yl)pyridine | HCID 13197538 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 3-Isopropyl-2-methyl-1-oxidopyridin-1-ium | HCID 23530578 | 94% |
Reaction Steps
A 50% solution of hydrogen peroxide (24.89 mL) was slowly added to a solution of 3-isopropyl-2-methyl-pyridine (24.5 g, 183 mmol) (Ishiguro et al. Yakugaku Zasshi 1958, 78, 220) in HOAc (280 mL). The mixture was warmed to 70° C. and stirred for 18 h, then cooled to room temperature and concentrated in vacuo to remove the majority of HOAc. The mixture was basified with a saturated solution of NaHCO3 to pH 12 and extracted with CH2Cl2 (3×150 mL). The combined organic layers were dried over Na2SO4 and concentrated in vacuo to afford 3-isopropyl-2-methyl-pyridine 1-oxide (26.05 g, 94%) as a yellow oil. 1H NMR (CDCl3) δ 1.24 (d, 6H, J=7.0 Hz), 2.56 (s, 3H), 3.13 (sep, 1H, J=7.0 Hz), 7.06-7.17 (m, 2H), 8.17 (d, 1H, J=6.6 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07863293B2 |
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| Source dataset | uspto-grants-2011_01 |
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| ORD ID | ord-6ee550914e4141d1b24044d38cd1b4b1 |
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| Source note | uspto-grants-2011_01 |
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