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.
以邻氯甲酸和对氧基胺为原料,经过胺的基化、芳胺的环化、N-烷基化、硫代化反应合成了N-丁基-2-氧基硫代吖啶酮。
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.
以邻氯甲酸和对氧基胺为原料,经过胺的基化、芳胺的环化、N-烷基化、硫代化反应合成了N-丁基-2-氧基硫代吖啶酮。
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