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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1466563Generated: November 1, 2026

m-Chloroperbenzoic acid → 5-Bromo-2-methylpyridin-1-ium-1-olate

https://huagongshe.com/reaction/1466563

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant5-Bromo-2-methylpyridineHCID 1201020—
SolventChloroformHCID 6212—
Product5-Bromo-2-methylpyridin-1-ium-1-olateHCID 817164—

Reaction Steps

A solution of 5-bromo-2-methylpyridine (2.0 g, 12 mmol, 1.0 eq) and m-chloroperoxybenzoic acid (70%, 2.89 g, 12.9 mmol, 1.1 eq) in 30 mL chloroform was stirred at room temperature for 4 hours. The reaction mixture was then partitioned between dichloromethane and 2 M aqueous sodium carbonate. The aqueous layer was extracted once more with dichloromethane, and the combined organic portions dried over magnesium sulfate and concentrated to give 5-bromo-2-methylpyridine 1-oxide. LCMS (ESI) m+H=189.0; 1H NMR (400 MHz, DMSO-d6) δ: 8.57 (s, 1H), 7.50 (d, 1H), 7.45 (d, 1H), 2.30 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999998B2
Source datasetuspto-grants-2015_04
ORD IDord-83e501746e8f4c44b13b9e813d006583
Source noteuspto-grants-2015_04