A new protocol for the oxidative bromination of aminoanthracene-9,10-dione, which is highly deactivated towards the electrophilic substitution is investigated. The peracid, nonanebis(peroxoic acid), possesses advantages such as better stability at room temperature, it is easy to prepare and non-shock sensitiv as compared to the conventional peracids. The present protocol has a broad scope for the bromination
Bedekar; Tilak; Venkataraman, Proceedings - Indian Academy of Sciences, Section A, 1948, vol. <A> 28, p. 236,248
作者:Bedekar、Tilak、Venkataraman
DOI:——
日期:——
Atack; Soutar, Journal of the Society of Chemical Industry, 1922, vol. 41, p. 170 A
作者:Atack、Soutar
DOI:——
日期:——
Efficient, facile metal free protocols for the bromination of commercially important deactivated aminoanthracene-9,10-diones
作者:Vilas V. Patil、Eknath M. Gayakwad、Khushbu P. Patel、Ganapati S. Shankarling
DOI:10.1016/j.tetlet.2017.05.078
日期:2017.6
Highly efficient, mild synthetic protocols were developed for the oxidative bromination of deactivated aminoanthracene-9,10-diones by using H2O2-HBr and m-CPBA-HBr in methanolic medium. Both the protocols offer excellent bromine atom economy, good conversion (100%) along with high yield (82-93%) and high purity of desired product. The N-alkylated amines undergo regio-selective bromination to give selective p-bromo product. The commercial availability of all the starting materials, simple reaction procedure and ease of work up, and easily amenable for scale up demonstrated commercial feasibility of both the protocols. (C) 2017 Elsevier Ltd. All rights reserved.
Bedekar et al., Proceedings - Indian Academy of Sciences, Section A, 1948, # 28, p. 236,247