Efficient one-stage procedure of Beckmann ketones rearrangement in the presence of hydroxylamine


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Resumo

Ketoximes formed from ketones in the presence of hydroxylamine and silica gel in formic acid undergo in situ the Beckmann rearrangement under mild conditions affording in high yields the corresponding amides. Unsymmetrical aromatic ketones, methyl aryl ketones, and methyl cyclohexyl ketone under these conditions form as a rule amides mixtures.

Sobre autores

V. Kuksenok

National Research Tomsk Polytechnic University

Autor responsável pela correspondência
Email: vera.kuksenok@mail.ru
Rússia, pr. Lenina 30, Tomsk, 634050

V. Shtrykova

National Research Tomsk Polytechnic University

Email: vera.kuksenok@mail.ru
Rússia, pr. Lenina 30, Tomsk, 634050

V. Filimonov

National Research Tomsk Polytechnic University

Email: vera.kuksenok@mail.ru
Rússia, pr. Lenina 30, Tomsk, 634050

S. Sidel’nikova

National Research Tomsk Polytechnic University

Email: vera.kuksenok@mail.ru
Rússia, pr. Lenina 30, Tomsk, 634050

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