纳米fe3o4催化合成吡喃吡唑衍生物

A. Cahyana, A. Mufidah
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引用次数: 0

摘要

吡喃吡唑是一种杂环有机化合物,其骨架是吡喃环,在邻位上被吡唑取代。以醛、肼、乙酰乙酸乙酯和丙二腈为前驱体,采用多组分反应法合成吡喃吡唑。吡吡唑的合成通过Knoevenagel缩合反应、Michael加成反应和环化反应进行。本研究以铁锈和废食用油为原料合成了纳米fe3o4。在纳米fe3o4催化剂用量为1% (w/w)的条件下,反应60 min内达到吡喃吡唑衍生物的最佳合成条件。在本研究中,苯甲醛、2-羟基苯甲醛和肉桂醛被用作醛的变体。结果表明,用纳米fe3o4在60 min内反应生成吡喃吡唑衍生物。利用FTIR、XRD和SEM-EDS等仪器对纳米fe3o4进行了表征。所得产物经FTIR、uv -可见、GC-MS表征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis of pyranopyrazole derivative compounds with nano-Fe3O4 catalyst
Pyranopyrazole is a heterocyclic organic compound in which the skeleton is a pyran ring substituted by pyrazole in the ortho position. Pyranopyrazole can be synthesized using aldehyde, hydrazine, ethyl acetoacetate, and malononitrile as precursors with a multicomponent reaction method. Synthesis of pyranopyrazole is carried out through the Knoevenagel condensation reaction, Michael’s addition, and cyclization. In this research, nano-Fe3O4 is synthesized from rust and used cooking oil. Synthesis of pyranopyrazole derivate compound reached the optimal condition within 60 min of the reaction with the amount of nano-Fe3O4 catalyst is 1 % (w/w). Benzaldehyde, 2-hydroxybenzaldehyde, and cinnamaldehyde are used in variations of aldehyde in this research. The results show that the reaction in 60 min using nano-Fe3O4 produces pyranopyrazole derivative compounds. The nano-Fe3O4 is characterized using FTIR, XRD, and SEM-EDS instruments. The resulting products are characterized by FTIR, UV-Visible, and GC-MS.
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