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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1043907Generated: October 31, 2026

Benzoyl Peroxide → 3-Bromo-2-(bromomethyl)-6-methoxy-4-methylpyridine

https://huagongshe.com/reaction/1043907

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant3-Bromo-6-methoxy-2,4-dimethylpyridineHCID 11241381—
SolventCarbon TetrachlorideHCID 5943—
Product3-Bromo-2-(bromomethyl)-6-methoxy-4-methylpyridineHCID 86686340—

Reaction Steps

A mixture of 3-bromo-6-methoxy-2,4-dimethylpyridine obtained in Preparation Example 22 (200 mg), NBS (165 mg) and benzoyl peroxide (6.73 mg) was heated under reflux in a carbon tetrachloride solvent (4 mL) for two hours. The reaction mixture was cooled to room temperature and then filtered. The resulting filtrate was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/n-heptane, 0% to 5%) to give the title compound (126 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08563565B2
Source datasetuspto-grants-2013_10
ORD IDord-590b71fa388c4a8fa285bcde42713374
Source noteuspto-grants-2013_10