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Acyloin condensation

From Biocrawler, the free encyclopedia.

In chemistry, the acyloin condensation is a reductive coupling of two carboxylic esters using metallic sodium to give an α-hydroxyketone, also known as an acyloin.

The reaction is most successful when R is aliphatic and inert, high-boiling solvents such as benzene and toluene are used.

References

  • Bouveault, L.; Loquin, R. Compt. Rend. 1905, 140, 1593.
  • Finley, K. T. Chem. Rev. 1964, 64, 573.

See also


Wikipedia (http://en.wikipedia.org/wiki/Main_Page) Acyloin_condensation (http://en.wikipedia.org/wiki/Acyloin_condensation) version history (http://en.wikipedia.org/w/index.php?title=Acyloin_condensation&action=history) GNU Free Documentation Lizenz (http://en.wikipedia.org/wiki/Wikipedia:Text_of_the_GNU_Free_Documentation_License) CC-by-sa (http://creativecommons.org/licenses/by-sa/2.5/)

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