以蜜胺甲醛树脂负载硫酸为固体酸催化剂,在微辐射下,利用苄基腈或芳基腈和叠氮化钠在N,N-二甲基甲酰胺(DMF)溶剂中的环加成反应,一步法制备得到5-取代四氮唑类化合物3a^3j,其结构经IR、1 H NMR和元素分析等表证;实验结果表明,在催化剂...以蜜胺甲醛树脂负载硫酸为固体酸催化剂,在微辐射下,利用苄基腈或芳基腈和叠氮化钠在N,N-二甲基甲酰胺(DMF)溶剂中的环加成反应,一步法制备得到5-取代四氮唑类化合物3a^3j,其结构经IR、1 H NMR和元素分析等表证;实验结果表明,在催化剂摩尔分数为20%,400 W,120℃,微波辐射下反应25~30min,目标化合物3a^3j收率为80%~92%,该方法具有操作简单、催化剂易回收和能多次使用等优点。展开更多
Zinc chloride is an efficient and safe catalyst in the [3 + 2] cycloaddition reaction of organic nitriles with sodium azide in solventless condition. The corresponding 5-substituted ^1H tetrazoles were obtained under...Zinc chloride is an efficient and safe catalyst in the [3 + 2] cycloaddition reaction of organic nitriles with sodium azide in solventless condition. The corresponding 5-substituted ^1H tetrazoles were obtained under mild conditions. This method can overcome disadvantages such as: the use of toxic metals and expensive reagents, drastic reaction conditions, water sensitivity and the presence of dangerous hydrazoic acid.展开更多
文摘以蜜胺甲醛树脂负载硫酸为固体酸催化剂,在微辐射下,利用苄基腈或芳基腈和叠氮化钠在N,N-二甲基甲酰胺(DMF)溶剂中的环加成反应,一步法制备得到5-取代四氮唑类化合物3a^3j,其结构经IR、1 H NMR和元素分析等表证;实验结果表明,在催化剂摩尔分数为20%,400 W,120℃,微波辐射下反应25~30min,目标化合物3a^3j收率为80%~92%,该方法具有操作简单、催化剂易回收和能多次使用等优点。
基金Research Council of K.N.Toosi University of Technology for partial financial support of this work
文摘Zinc chloride is an efficient and safe catalyst in the [3 + 2] cycloaddition reaction of organic nitriles with sodium azide in solventless condition. The corresponding 5-substituted ^1H tetrazoles were obtained under mild conditions. This method can overcome disadvantages such as: the use of toxic metals and expensive reagents, drastic reaction conditions, water sensitivity and the presence of dangerous hydrazoic acid.