Efficient and selective bromination of acetophenones
Keywords:
Efficient, acetophenones, EthylbenzeneAbstract
Acetophenone is recovered as a by-product of the oxidation of ethylbenzene to
ethylbenzene hydroperoxide. Ethylbenzene hydroperoxide is an intermediate in the commercial
production of propylene oxide via the propylene oxide - styrene co-product process.[1]
Ethylbenzene hydroperoxide is primarily converted to 1-phenylethanol (α-methylbenzyl alcohol)
in the process with a small amount of by-product acetophenone. Acetophenone is recovered or
hydrogenated to 1-phenylethanol which is then dehydrated to produce styrene.
References
ustrative procedure for chlorination of an aromatic compound: Edward R. Atkinson, Donald M. Murphy, and James E. Lufkin (1951). "dl-4,4′,6,6′-Tetrachlorodiphenic Acid". Organic Syntheses.; Collective Volume, 4, p. 872
Organic chemistry by Jonathan Clayden, Nick Grieves, Stuart Warren, Oxford University Press.
Synthesis of essential drugs, Ruben Vardanyan, Victor Hruby; Elsevier 2005 ISBN 0-444-52166-6.
Gordon W. Gribble “The diversity of naturally occurring organobromine compounds” Chemical Society Reviews, 1999, volume 28, pages 335–346.
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