Efficient and selective bromination of acetophenones

Authors

  • Dr Poonam Asstt. Professor (Chemistry)DR. BRA Govt. College, Kaithal

Keywords:

Efficient, acetophenones, Ethylbenzene

Abstract

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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Published

2018-03-30

How to Cite

Dr Poonam. (2018). Efficient and selective bromination of acetophenones. Innovative Research Thoughts, 4(2), 61–65. Retrieved from https://irt.shodhsagar.com/index.php/j/article/view/472