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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1945589Generated: October 28, 2026

m-Chloroperbenzoic acid → 2-Bromo-5-methylpyridine 1-oxide

https://huagongshe.com/reaction/1945589

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant2-Bromo-5-methylpyridineHCID 564216—
SolventChloroformHCID 6212—
Product2-Bromo-5-methylpyridine 1-oxideHCID 1317873791.7%

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 2-bromo-5-methylpyridine (2.0 g, 11.6 mmol) and 3-chloroperbenzoic acid (3.0 g, 14.8 mmol) in chloroform (7 mL) was stirred at 50° C. for 3 hours, cooled down to room temperature and filtered. The filtrate was concentrated under reduced pressure to give a residue that was purified by flash chromatography (Si—PPC, MeOH:EtOAc, gradient 0:100 to 10:90) to give 2-Bromo-5-methylpyridine 1-oxide as a white solid (2.0 g, 91%). 1H NMR (400 MHz, CHCl3-d): δ 8.24 (s, 1 H); 7.52 (d, J=8.3 Hz, 1 H); 6.93 (d, J=8.33 Hz, 1 H); 2.29 (s, 3 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394796B2
Source datasetuspto-grants-2013_03
ORD IDord-d2edd791902844359b0a36349c17f1cf
Source noteuspto-grants-2013_03