Synthesis of 5-amino-6-(nitro-NNO-azoxy)-1,2,3,4-tetrazine 1,3-dioxide
- Authors: Klenov M.S.1, Leonov N.E.1,2, Guskov A.A.1, Churakov A.M.1, Strelenko Y.A.1, Tartakovsky V.A.1
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Affiliations:
- N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
- Mendeleev University of Chemical Technology of Russia
- Issue: Vol 68, No 9 (2019)
- Pages: 1798-1800
- Section: Brief Communications
- URL: https://journal-vniispk.ru/1066-5285/article/view/243489
- DOI: https://doi.org/10.1007/s11172-019-2628-7
- ID: 243489
Cite item
Abstract
A reaction of 5-amino-6-(tert-butyl-NNO-azoxy)-1,2,3,4-tetrazine 1,3-dioxide with nitronium tetrafluoroborate affords 5-amino-6-(nitro-NNO-azoxy)-1,2,3,4-tetrazine 1,3-dioxide, which can be of interest as an energetic compound. A plausible mechanism of its formation involves substitutive nitration of the tert-butyl group.
About the authors
M. S. Klenov
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
Author for correspondence.
Email: klenov@ioc.ac.ru
Russian Federation, 47 Leninsky prosp., Moscow, 119991
N. E. Leonov
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences; Mendeleev University of Chemical Technology of Russia
Email: klenov@ioc.ac.ru
Russian Federation, 47 Leninsky prosp., Moscow, 119991; 9 Miusskaya pl., Moscow, 125047
A. A. Guskov
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
Email: klenov@ioc.ac.ru
Russian Federation, 47 Leninsky prosp., Moscow, 119991
A. M. Churakov
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
Email: klenov@ioc.ac.ru
Russian Federation, 47 Leninsky prosp., Moscow, 119991
Yu. A. Strelenko
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
Email: klenov@ioc.ac.ru
Russian Federation, 47 Leninsky prosp., Moscow, 119991
V. A. Tartakovsky
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
Email: klenov@ioc.ac.ru
Russian Federation, 47 Leninsky prosp., Moscow, 119991
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