The Hayashi rearrangement is the chemical reaction of ortho-benzoylbenzoic acids catalyzed by sulfuric acid or phosphorus pentoxide.[1][2]

The Hayashi rearrangement
The Hayashi rearrangement

This reaction proceeds through electrophilic acylium ion attack with a spiro intermediate.[3][4]

Hayashi mechanism

References

  1. ^ Mosuke Hayashi (1927). "A new isomerism of halogenohydroxybenzoyltoluic acids". Journal of the Chemical Society: 2516. doi:10.1039/JR9270002516.
  2. ^ Mosuke Hayashi (1930). "A new isomerism of halogenohydroxybenzoyltoluic acids. Part II. 2-(5-Chloro-2-hydroxybenzoyl)-5(4?)-methylbenzoic acid". Journal of the Chemical Society: 1513. doi:10.1039/JR9300001513.; p. 1520 doi:10.1039/JR9300001520; p. 1524doi:10.1039/JR9300001524
  3. ^ The Hayashi Rearrangement of Substituted o-Benzoylbenzoic Acids Reuben B. Sandin, Russell Melby, Robert Crawford, and Donald McGreer J. Am. Chem. Soc. 1956 pp 3817 - 3819; doi:10.1021/ja01596a069
  4. ^ Name Reactions: A Collection of Detailed Reaction Mechanisms By Jie Jack Li Published 2003 Springer ISBN 3-540-40203-9
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