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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1644002Generated: October 30, 2026

Carbon Tetrachloride → 2-Bromo-5-bromomethylpyridine

https://huagongshe.com/reaction/1644002

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon TetrachlorideHCID 5943—
ReactantN-bromobutanimideHCID 67184—
Reactant2-Bromo-5-methylpyridineHCID 564216—
CatalystBenzoyl PeroxideHCID 7187—
Product2-Bromo-5-bromomethylpyridineHCID 6424660105.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 2-Bromo-5-methylpyridine (3.1 g, 17.4 mmol) in carbon tetrachloride (40 mL, 400 mmol) was added benzoyl peroxide (230 mg, 950 μmol) and NBS (3.4 g, 19.2 mmol). The resulting mixture was heated at reflux overnight. The mixture was cooled at 0° C. and the NBS was removed by filtration. The filtrate was concentrated to yield 2-bromo-5-bromomethylpyridine (4.6 g), which was used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119634B2
Source datasetuspto-grants-2012_02
ORD IDord-46e10c9235364468909acbafc27f91bd
Source noteuspto-grants-2012_02