HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1775369Generated: November 1, 2026
m-Chloroperbenzoic acid → 3-Bromo-2-methylpyridine N-oxide
https://huagongshe.com/reaction/1775369
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 3-Bromo-2-methylpyridine | HCID 1201003 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Bromo-2-methylpyridine N-oxide | HCID 14402952 | 81% |
Reaction Steps
To a solution of 3-bromo-2-methylpyridine (5 g, 29.1 mmol) in DCM (50 ml) was added portionwise at 0° C. m-chloroperbenzoic acid (70%, 8.6 g, 34.9 mmol). The solution was stirred at 0° C. for three hours and then at room temperature overnight. The mixture was filtered, the residue was washed with DCM and the combined DCM phases were quenched with a 10% solution of sodium thiosulfate. The phases were separated, the organic phase was washed with a saturated solution of sodium bicarbonate and brine, dried (sodium sulfate) and concentrated under reduced pressure. The residue was purified by column chromatography (silica, diethyl ether, then DCM/methanol 95:5) to yield 4.44 g (23.6 mmol, yield 81%) MS (multi-mode) m/z=190.0 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09260441B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-9b821ed472494f36a9b360b4039bd2ee |
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| Source note | uspto-grants-2016_02 |
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