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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234766Generated: October 25, 2026

Azobisisobutyronitrile → 4-(Bromomethyl)-2-chloro-1-iodobenzene

https://huagongshe.com/reaction/234766

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzobisisobutyronitrileHCID 6547—
ReactantN-bromobutanimideHCID 67184—
Reactant2-Chloro-1-iodo-4-methylbenzeneHCID 2757618—
SolventCarbon TetrachlorideHCID 5943—
Product4-(Bromomethyl)-2-chloro-1-iodobenzeneHCID 54255292—

Reaction Steps

A suspension of 40.4 g (160 mmol) of the compound from Example XXXI in 400 ml of carbon tetrachloride, 31.3 g of N-bromosuccinimide (176 mmol) and 2.63 g of azobisisobutyronitrile (16 mmol) is heated under reflux overnight. After cooling, the precipitate is filtered off with suction and washed with carbon tetrachloride. The combined filtrates are concentrated and the residue is further reacted in the crude state.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05596006
Source datasetuspto-grants-1997_01
ORD IDord-2d9396fe463b42afb56f4077c7234a30
Source noteuspto-grants-1997_01