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  Home > JCE Print > Journal of Chemical Education > Issues > 1996  > March  >
Laboratory Experiments
Bromination of Acetanilide
Paul F. Schatz
University of Wisconsin-Madison, Madison, WI 53706
Cover
March 1996
Vol. 73 No. 3
p. 267
Abstract
A general procedure for bromination of aromatic compounds activated with electron donating substituents such as acetamido, hydroxyl, or ether groups is described. Bromine is generated in situ from potassium bromate and hydrobromic acid. This procedure avoids the hazards associated with direct handling of bromine or bromine solutions. The results from seven aromatic ethers and anilides are reported.
More Information
*  Citation
 Schatz, Paul F. J. Chem. Educ. 1996 73 267.
*  Keywords
*  History
 Created:
Last Updated:		 9/23/1999
5/22/2006
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