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.

Авторы
Andrievskii A.M.1 , Gorelik M.V.1 , Linko R.V. 2 , Grachev M.K.3
Номер выпуска
10
Язык
Английский
Страницы
1474-1481
Статус
Опубликовано
Том
49
Год
2013
Организации
  • 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
Цитировать
Поделиться

Другие записи

Slivkin A.I., Lapenko V.L., Bychuk A.I., Suslina S.N., Slivkin D.A., Kornienko S.V., Belenova A.S.
Бюллетень экспериментальной биологии и медицины Клеточные технологии в биологии и медицине. New York Consultants BureauSpringer / Автономная некоммерческая организация Издательство Российской академии медицинских наук. Том 155. 2013. С. 764-766