Synthesis of 1,3,4,6-tetraoxo compounds


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Abstract

The two-step method of synthesis of 1,3,4,6-tetraoxocompounds with different terminal substituents is developed. By condensation of alkyl methyl ketones with dimethyl oxalate new 1,6-dialkyl-substituted 1,3,4,6-tetraoxohexanes are obtained. The esters of 3,4,6-trioxoalkanoic acids are synthesized by the condensation reaction of alkyl acetates with dialkyl oxalates and alkyl methyl ketones. By the reaction of ethyl acetate with diethyl oxalate and methyl acetate the mixed diester of 3,4-dioxo-1,6-hexanedioic (ketipic) acid has been first prepared. Specific structural features of the synthesized compounds are discussed basing on the data of the IR, NMR, and XRD diffraction (XRD) analysis.

About the authors

P. P. Mukovoz

Orenburg Branch

Author for correspondence.
Email: mpp27@mail.ru
Russian Federation, pr. Pobedy 75, Orenburg, 460018

V. O. Koz’minykh

Perm State Humanitary Pedagogical University

Email: mpp27@mail.ru
Russian Federation, Perm

A. V. Gorbunova

Orenburg State University

Email: mpp27@mail.ru
Russian Federation, Orenburg

P. A. Slepukhin

I.Ya. Postovskii Institute of Organic Synthesis; Ural Federal University named after the first President of Russia B.N. Yeltsin

Email: mpp27@mail.ru
Russian Federation, Yekaterinburg; Yekaterinburg

O. S. El’tsov

Ural Federal University named after the first President of Russia B.N. Yeltsin

Email: mpp27@mail.ru
Russian Federation, Yekaterinburg

I. N. Ganebnykh

I.Ya. Postovskii Institute of Organic Synthesis; Ural Federal University named after the first President of Russia B.N. Yeltsin

Email: mpp27@mail.ru
Russian Federation, Yekaterinburg; Yekaterinburg

A. V. Kuzmin

Institute of Solid State Physics of Russian Academy of Sciences

Email: mpp27@mail.ru
Russian Federation, Chernogolovka


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