N butyl 2 ethoxy thioacridone was prepared from o chloro benzoic acid and p phenetidine by means of Ullman reaction,cyclization,N alkylation and sulfurization.
以邻氯苯甲酸和对乙氧基苯胺为原料,经过胺的苯基
、二芳胺的环、N-烷基、
代反应合成了N-丁基-2-乙氧基代吖啶酮。
;作用N butyl 2 ethoxy thioacridone was prepared from o chloro benzoic acid and p phenetidine by means of Ullman reaction,cyclization,N alkylation and sulfurization.
以邻氯苯甲酸和对乙氧基苯胺为原料,经过胺的苯基、二芳胺的环、N-烷基、代反应合成了N-丁基-2-乙氧基代吖啶酮。
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