Reaction type Substitution reaction | Organic Chemistry Portal wohl-ziegler-reaction | |
Named after Alfred Wohl
Karl Ziegler | ||
The Wohl–Ziegler reaction is a chemical reaction that involves the allylic or benzylic bromination of hydrocarbons using an N-bromoimide and a radical initiator.
Best yields are achieved with N-bromosuccinimide in carbon tetrachloride solvent. Several reviews have been published.
In a typical setup a stoichiometric amount of N-bromosuccinimide solution and a small quantity of initiator are added to a solution of the substrate in CCl4, and the reaction mixture is stirred and heated to the boiling point. Initiation of the reaction is indicated by more vigorous boiling; sometimes the heat source may need to be removed. Once all N-bromosuccinimide (which is denser than the solvent) has been converted to succinimide (which floats on top) the reaction has finished.