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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1471761Generated: November 1, 2026

Azobisisobutyronitrile → 6-(Bromomethyl)pyridine-3-carbonitrile

https://huagongshe.com/reaction/1471761

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
Reactant6-Methylpyridine-3-carbonitrileHCID 281995—
SolventCarbon TetrachlorideHCID 5943—
Product6-(Bromomethyl)pyridine-3-carbonitrileHCID 2192777637.5%

Reaction Conditions

Temperature85 °C

Reaction Steps

Into a 250-mL round-bottom flask, was placed a solution of 6-methylpyridine-3-carbonitrile (8 g, 67.72 mmol, 1.00 equiv) in CCl4 (125 mL). N-Bromosuccinimide (13.4 g, 75.29 mmol, 1.10 equiv), and AIBN (480 mg, 2.92 mmol, 0.04 equiv) were added to the reaction solution. The resulting solution was stirred for 5 h at 85° C. The resulting mixture was concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1:5) as eluent to yield 5 g (37%) of 6-(bromomethyl)pyridine-3-carbonitrile as a beige solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09012450B2
Source datasetuspto-grants-2015_04
ORD IDord-bf24625a23ea48dbb7471a90ec8a2e6e
Source noteuspto-grants-2015_04