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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2187871Generated: November 1, 2026

Azobisisobutyronitrile → 4-Cyano-3-fluorobenzyl bromide

https://huagongshe.com/reaction/2187871

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
Reactant2-Fluoro-4-methylbenzonitrileHCID 2778443—
SolventCarbon TetrachlorideHCID 5943—
Product4-Cyano-3-fluorobenzyl bromideHCID 2778466—

Reaction Steps

To a solution of 4-cyano-3-fluorotoluene, as described above in Step C, (5.0 g, 37.0 mmol) in carbon tetrachloride (300 mL) was added N-bromosuccinimide (7.57 g, 42.6 mmol) and 2,2′-azobisisobutyronitrile (610 mg, 3.7 mmol). The reaction mixture was heated to reflux under argon for 24 hrs, then cooled to room temperature, filtered, and concentrated under reduced pressure. The residue was purified by silica gel chromatography, eluting with a gradient of hexane −4% to 7% EtOAc, to yield the titled product as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06410534B1
Source datasetuspto-grants-2002_06
ORD IDord-97518aec97e84e2b8a624be3e61cd0dc
Source noteuspto-grants-2002_06