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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1502338Generated: October 31, 2026

m-Chloroperbenzoic acid → 2-Bromo-3-methylpyridine 1-oxide

https://huagongshe.com/reaction/1502338

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant2-Bromo-3-methylpyridineHCID 220832—
SolventDichloromethaneHCID 6344—
Product2-Bromo-3-methylpyridine 1-oxideHCID 1337667878%

Reaction Steps

A mixture of 2-bromo-3-methyl-pyridine (1000 mg, 5.81 mmol) and 3-chloroperoxybenzoic acid (2150 mg, 8.72 mmol) in dichloromethane (8 mL) was stirred overnight at room temperature. The reaction mixture was diluted with DCM (50 mL) and washed with saturated aqueous sodium thiosulfite (10 mL) followed by saturated aqueous sodium bicarbonate (10 mL). The organic layer was separated, dried over sodium sulfate, filtered and concentrated in vacuo to provide a residue that was purified by flash chromatography (4 g, Silica, 0-10% methanol in DCM). Desired fractions were combined and evaporated in vacuo to afford the title compound as white solid (851 mg, 78%), which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206175B2
Source datasetuspto-grants-2015_12
ORD IDord-43008bd10bab422d8d4f61f98029e386
Source noteuspto-grants-2015_12