Reduction of Oximes

Authors

  • Surapol Patharakorn Department of Chemistry, Faculty of Science, Kasetsart University, Bangkok 10900, Thailand
  • Chongkolnee Kaewsriprakai Department of Chemistry, Faculty of Science, Kasetsart University, Bangkok 10900, Thailand

Keywords:

reduction, oximes, sodium borohydride

Abstract

The reduction of 8 oximes (6 ketoximes and 2 aldoximes) with sodium borohydride under acidic condition was studied. The reduction of certain oximes, particularly cyclohexanone oxime, gave corresponding N-monosubstituted hydroxylamines in comparable yield with the reduction with sodium cyanoborohydride under the same conditon. Aromatic ketoxime and aldoximes were poorly reduced and corresponding hydroxylamines were not obtained.

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Published

1998-03-31

How to Cite

Patharakorn, Surapol, and Chongkolnee Kaewsriprakai. 1998. “Reduction of Oximes”. Agriculture and Natural Resources 32 (1). Bangkok, Thailand:64-72. https://li01.tci-thaijo.org/index.php/anres/article/view/240555.

Issue

Vol. 32 No. 1 (1998): January-March

Section

Research Article

License

online 2452-316X print 2468-1458/Copyright © 2022. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/),
production and hosting by Kasetsart University of Research and Development Institute on behalf of Kasetsart University.