Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2220258Generated: October 31, 2026

Azobisisobutyronitrile → 2-Bromo-5-bromomethylpyridine

https://huagongshe.com/reaction/2220258

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
Reactant2-Bromo-5-methylpyridineHCID 564216—
Reactant2-Bromo-5-(dibromomethyl)pyridineHCID 56605143—
SolventCarbon TetrachlorideHCID 5943—
Product2-Bromo-5-bromomethylpyridineHCID 642466043%

Reaction Steps

To a stirred slurry of 10.320 g (60.0 mmol) of 5-methyl-2-bromopyridine and 5.339 g (30.0 mmol, 0.5 eq) of recrystallized N-bromosuccinimide in 150 mL of carbon tetrachloride was added 200 mg of AIBN. The reaction mixture was purged twice with argon and evacuated and set to reflux under argon. After 90 min, the reaction mixture was cooled to room temperature, filtered and the filtrate concentrated to give a yellow oil. Proton NMR indicated that the mixture contains 53% (mol) unreacted 5-methyl-2-bromopyridine, 43% of the title product and 4% of 2-bromo-5-(dibromomethyl)pyridine. The mixture was used immediately without further purification for the following procedure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07417028B2
Source datasetuspto-grants-2008_08
ORD IDord-bab0f42f20454dd68f18e8061b88e7ab
Source noteuspto-grants-2008_08