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
Issue number
10
Language
English
Pages
1474-1481
State
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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