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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 343964Generated: October 26, 2026

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

https://huagongshe.com/reaction/343964

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 azobisiso-butyronitrile (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 numberUS05863930
Source datasetuspto-grants-1999_01
ORD IDord-26a5b0d63efe451aab8d09bee8e8962a
Source noteuspto-grants-1999_01