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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 493401Generated: October 27, 2026

Azobisisobutyronitrile → 3-Bromo-6-(bromomethyl)pyridazine

https://huagongshe.com/reaction/493401

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
Reactant3-Bromo-6-methylpyridazineHCID 11959086—
SolventCarbon TetrachlorideHCID 5943—
Product3-Bromo-6-(bromomethyl)pyridazineHCID 5768029730%

Reaction Steps

A solution of 1.00 g (5.78 mmol) of 3-bromo-6-methylpyridazine and 1.03 g (5.79 mmol, 1.0 eq) of recrystallized N-bromosuccinimide in 20 mL of carbon tetrachloride was added 95 mg of AIBN. The reaction mixture was purged twice with argon and evacuated and set to reflux under argon. After 3 h, the reaction mixture was cooled to room temperature, filtered and the filtrate was concentrated to give a yellow oil. The mixture was directly purified by silica gel chromatography using hexanes/dichloromethane (1:9) as eluant (5×12 cm column), to give a colorless oil, 444 mg, 30% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07534763B2
Source datasetuspto-grants-2009_05
ORD IDord-40267066fa0647ddb8fcea80faa7af00
Source noteuspto-grants-2009_05