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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1025717Generated: November 3, 2026

Benzoyl Peroxide → 2-Bromo-5-bromomethylpyridine

https://huagongshe.com/reaction/1025717

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant2-Bromo-5-methylpyridineHCID 564216—
SolventCarbon TetrachlorideHCID 5943—
Product2-Bromo-5-bromomethylpyridineHCID 6424660—

Reaction Steps

2-Bromo-5-methylpyridine (5.00 g, 29.1 mmoles) and N-bromosuccinimide (5.22 g, 29.3 mmoles) were dissolved in carbon tetrachloride (40 mL) under nitrogen. Benzoyl peroxide (0.35 g, 1.4 mmoles) was added and the mixture heated at reflux for four hours. The mixture was cooled to room temperature, filtered, and washed with NaHCO3/H2O. The mixture was adsorbed onto silica gel and then chromatographed. eluting with a gradient of hexane to 10% ethyl acetate/hexane. Pure fractions were combined and concentrated to provide the desired mono-brominated product as a pale yellow solid, 3.60 g (49%). LC/MS (positive ion) m/z=249.8, 251.8, 253.8, (M+H)+. Step B

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729063B2
Source datasetuspto-grants-2014_05
ORD IDord-b9dbc0feb61e434697ed75e7ff8da912
Source noteuspto-grants-2014_05