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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant3-Bromo-2-methylpyridineHCID 1201003—
SolventDichloromethaneHCID 6344—
Product3-Bromo-2-methylpyridine N-oxideHCID 1440295281%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260441B2
Source datasetuspto-grants-2016_02
ORD IDord-9b821ed472494f36a9b360b4039bd2ee
Source noteuspto-grants-2016_02