Reactions of 9-chloro-1,10-anthraquinone 1-dichlorophosphorylimine with N- and C-nucleophiles
作者:M. V. Gorelik、S. P. Titova、T. Kh. Gladysheva
DOI:10.1007/bf02503488
日期:1998.6
formed in the reaction of 1-amino-9,10-anthraquinone with PCl5 followed by dehydrochlorination reacts with primary amines with substitution of chlorine atoms. In the case of aliphatic amines, the reaction occurs further concurrently in two directions: the addition of the amine molecule with the formation of 9,9-di(alkylamino) derivatives of the anthrone and the substitution of hydrogen atom at position
摘要9-Chloro-1,10-anthraquinone 1-amino-9,10-anthraquinone 与PCl5 反应生成1-二氯磷酰亚胺,然后脱氯化氢与氯原子取代的伯胺反应。在脂肪胺的情况下,反应在两个方向上进一步同时发生:胺分子的加成与蒽酮的 9,9-二(烷基氨基)衍生物的形成和 4 位氢原子的取代与形成1,10-蒽醌1-亚胺的4,9-二(烷基氨基)衍生物。在芳香胺的情况下,1-氨基-9,10-蒽醌9-芳基亚胺是最终产物。