Bromination of deactivated polycyclic aromatic nitro compounds

Bromination of 2,7-dinitro-9,10-phenanthrenequinone, 2,5-dinitro-9,10- phenanthrenequinone, and 2,4,7-trinitrofluorenone with bromine in concentrated sulfuric acid in the presence of acetic acid gave, respectively, 4-bromo-2,7-dinitro-9,10-phenanthrenequinone, 2-bromo-4,7-dinitro-9,10- phenanthrenequinone, and 5-bromo-2,4,7-trinitrofluorenone. No bromination occurred in the absence of nitric acid. The same brominated polynitro compounds can be obtained under analogous conditions directly from unsubstituted 9,10-phenanthrenequinone and fluorenone. © 2013 Pleiades Publishing, Ltd.

Authors
Andrievskii A.M.1 , Gorelik M.V.1 , Linko R.V. 2 , Grachev M.K.3
Number of issue
10
Language
English
Pages
1474-1481
Status
Published
Volume
49
Year
2013
Organizations
  • 1 State Scientific Center, Research Institute of Organic Intermediate Products and Dyes, ul. Bol'shaya Sadovaya 1/4, Moscow 123995, Russian Federation
  • 2 Peoples' Friendship University of Russia, Moscow, Russian Federation
  • 3 Moscow State Pedagogical University, Moscow, Russian Federation
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Slivkin A.I., Lapenko V.L., Bychuk A.I., Suslina S.N., Slivkin D.A., Kornienko S.V., Belenova A.S.
Bulletin of Experimental Biology and Medicine. New York Consultants BureauSpringer / Автономная некоммерческая организация Издательство Российской академии медицинских наук. Vol. 155. 2013. P. 764-766