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Safer and Convenient Synthesis of 3,4-Dicyanofuroxan

机译:更安全,方便地合成3,4-二辛糖呋喃昔南

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摘要

A safer, convenient, cost-effective, and scalable synthesis for 3,4-dicyanofuroxan (C4N4O2) is described. Dropwise treatment of a well-stirred suspension of cyanoacetic acid in dichloromethane with concentrated mixed acid (HNO3/H2SO4) affords dicyanofuroxan in 72% yield and in 84% purity after liquid chromatography analysis. Single crystal X-ray diffraction studies further confirm the product and yield its molecular conformation and crystal packing. During the dropwise addition of mixed acid, self-heating occurs, and this event is necessary for the reaction to adequately proceed. However, such self-heating is limited to the refluxing temperature of dichloromethane. This new method supersedes the previous methods used to synthesize dicyanofuroxan, which were low-yielding and of significantly lower purity, irreproducible, relied on expensive reagents, and suffered from dangerous exothermic profiles.
机译:描述了一种更安全,方便,成本效益和可扩展合成3,4-二氰诺昔诺(C4N4O2)。 滴加在二氯甲烷中搅拌搅拌的搅拌溶液搅拌的浓缩混合酸(HNO3 / H 2 SO 4),得到二氰呋脲,在液相色谱分析后以72%的产率和84%纯度为84%。 单晶X射线衍射研究进一步证实了产物并产生其分子构象和晶体包装。 在滴加混合酸的过程中,发生自加热,并且该事件是对反应进行充分进行的必要条件。 然而,这种自加热仅限于二氯甲烷的回流温度。 这种新方法取代了以合成二氰脲氧基的先前方法,该方法是低产生的,并且具有明显较低的纯度,Irreproyum,依赖于昂贵的试剂,并且遭受危险的放热曲线。

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