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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2204331Generated: October 29, 2026

Azobisisobutyronitrile → 4-Bromo-2-(bromomethyl)-5-methoxypyridine

https://huagongshe.com/reaction/2204331

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantBenzoyl PeroxideHCID 7187—
ReactantN-bromobutanimideHCID 67184—
Reactant4-broMo-5-Methoxy-2-MethylpyridineHCID 73554829—
SolventCarbon TetrachlorideHCID 5943—
SolventEthyl AcetateHCID 8857—
Product4-Bromo-2-(bromomethyl)-5-methoxypyridineHCID 86703138—

Reaction Steps

A solution of 4-bromo-5-methoxy-2-methyl-pyridine (Step AL3) (1.9 g, 9.4 mmol), NBS (1.8 g, 9.9 mmol), AIBN (15 mg, 0.094 mmol) and benzoyl peroxide (23 mg, 0.094 mmol) in CCl4 (2 mL) was stirred at rt for 18 h. The reaction mixture was dissolved in EtOAc and extracted with a saturated aqueous solution of NaHCO3, washed with brine, dried (Na2SO4), filtered and concentrated. The crude product was purified by silica gel column chromatography (hexane/EtOAc, 100:0→70:30). ESI-MS: tR=0.90 min, [M+H]+ 281.9 (LC-MS 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365576B2
Source datasetuspto-grants-2016_06
ORD IDord-1b4ec48eec4b4c8f8fa7644ddc043d61
Source noteuspto-grants-2016_06