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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2286356Generated: October 30, 2026

Azobisisobutyronitrile → 1-Azido-4-(bromomethyl)benzene

https://huagongshe.com/reaction/2286356

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
Reactant1-Azido-4-methylbenzeneHCID 137430—
SolventCarbon TetrachlorideHCID 5943—
Product1-Azido-4-(bromomethyl)benzeneHCID 11816667104.7%

Reaction Steps

A mixture of p-azidotoluene (3.9 g), N-bromosuccinimide (5.5 g) and azobisisobutyronitrile (1.0 g) in carbon tetrachloride (30 ml) was heated under reflux in the dark under nitrogen for 18 h. The reaction mixture was allowed to cool to room temperature and the solvent was removed in vacuo. The residue was dissolved in ether (50 ml) and filtered. Evaporation of solvent gave an oil (6.5 g) which was chromatographed on silica gel (200 g, Merck 7734). Elution with petroleum ether (b.p.40°-60°) gave the title compound as an oil (2.37 g). I.R. (Neat) 2120 cm-1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04265891
Source datasetuspto-grants-1981_05
ORD IDord-6b7cdc4d21a547b68c508b77adbb132d
Source noteuspto-grants-1981_05