Fe3O4磁性催化剂绿色合成肉桂基苯乙酮化合物及表征

Dori Fitria, A. Cahyana, A. R. Liandi
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引用次数: 1

摘要

肉桂醛是一种在肉桂植物表皮中发现的化合物,具有多种生物活性。本研究以海藻提取物为多相催化剂,用Fe3O4对化合物肉桂醛进行了改性。以FeCl3和马尾藻提取物为天然还原剂合成了Fe3O4-MNPs。考察了Fe3O4在回流法合成的肉桂醛与芳香酮反应中的催化性能。通过FTIR测量官能团的振动,HNMR和CNMR分析确定H和C原子,对合成的化合物进行了结构分析和解析。经红外光谱、质子和碳核磁共振分析,合成产物为肉桂基苯二酮,命名为1,5二苯基苯-2,4-二烯-1- 1。最佳反应条件为催化剂浓度为10% w/w,反应时间为5小时,收率为36%。该反应的产率高于无催化剂反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Green Synthesis and Characterization of Cinnamylideneacetophenone Compound Using Fe3O4 Magnetic as Catalyst
Cinnamaldehyde is a compound found in the skin of cinnamon plants which has various bioactivity. In this study, the compound cinnamaldehyde was modified with the help of Fe3O4 which was synthesized with the help of seaweed extract as a heterogeneous catalyst. Fe3O4-MNPs are synthesized using FeCl3 and Sargassum filipendula extracts as their natural reducing agents. The catalytic ability of Fe3O4 was evaluated in the reaction between cinnamaldehyde and aromatic ketone compounds synthesized by the reflux method. Structure Analysis and elucidation of the synthesized compounds were carried out by measuring the vibrations of the functional groups by FTIR, and the determination of H and C atoms by HNMR and CNMR analysis. The FTIR, proton and carbon NMR analysis have identified that the synthesized product was cinnamylideneacetophenone by the name 1,5diphenylpyenta-2,4-dien-1-one. The optimum conditions were obtained at a catalyst concentration of 10% w/w for five hours with a yield of 36%. The yield of this reaction was better than the reaction without a catalyst.
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