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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1106959Generated: October 26, 2026

Azobisisobutyronitrile → 2-(1-Naphthyl)benzyl bromide

https://huagongshe.com/reaction/1106959

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
Reactant(Methylphenyl)naphthaleneHCID 3016790—
SolventCarbon TetrachlorideHCID 5943—
Product2-(1-Naphthyl)benzyl bromideHCID 11077333—

Reaction Steps

114 g (0.52 mol) of 6 and 103 g (0.58 mol) of N-bromosuccinimide were dissolved at room temperature in 2000 cm3 of carbon tetrachloride, admixed with 3 g of azobisisobutyronitrile and heated under reflux for 4 hours. The precipitated succinimide was filtered off, the solvent was removed under reduced pressure and the residue was purified by filtration through 1000 g of silica gel (hexane/methylene chloride 9:1). This gave 141 g (82%) of 7 as a colorless lacrymatory oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06057408
Source datasetuspto-grants-2000_05
ORD IDord-ff5f8810cbf84b7b89c55966288d3739
Source noteuspto-grants-2000_05