116-82-5Relevant articles and documents
Halogenation reactions in biodegradable solvent: Efficient bromination of substituted 1-aminoanthra-9,10-quinone in deep eutectic solvent (choline chloride:urea)
Phadtare, Sunanda Balaso,Shankarling, Ganapati Subray
, p. 458 - 462 (2010)
A simple ammonium deep eutectic solvent was used as a dual catalyst and environmentally benign reaction medium for the bromination of 1-aminoanthra-9,10-quinone, eliminating the need for volatile organic solvents and concentrated acids like H2SO4 as solvents or catalysts. This simple ammonium deep eutectic solvent, easily synthesized from choline chloride and urea, is relatively inexpensive and biodegradable, making it applicable for industrial applications. The deep eutectic solvent was easily separated and reused without loss of activity, and thus provides a good alternative for industrial bromination of 1-aminoanthra-9,10-quinone.
CHARACTERISTICS OF THE ALKOXYLATION OF HALOGENO-6-OXO-6H-ANTHRAISOXAZOLES
Es'kin, A. P.,Gornostaev, L. M.,Zeibert, G. F.,Bogdanchikov, G. A.,El'tsov, A. V.
, p. 162 - 167 (2007/10/02)
The alkylation of 6-oxo-6H-anthraisoxazoles containing a chlorine or bromine atom at position 3 and also a bromine at position 5 takes place with substitution of the halogen or hydrogen, depending on the structure of the alkoxide ion and the type of halogen.
Process for the preparation of 1-amino-2-bromo-4-hydroxyanthraquinone
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, (2008/06/13)
1-Amino-2-bromo-4-hydroxyanthraquinone is obtained in good yields and in an environmentally acceptable manner by bromination of 1-aminoanthraquinone in 2 to 5 times the quantity by weight of 80 to 98% strength sulphuric acid and using 1.1-1.5 mole of bromine under elevated pressure.