1. 毕业设计（论文）的内容和要求

以氯化钯为催化剂，三苯基膦为配体，对甲苯磺酸为助催化剂，通过2,5-二氢呋喃与芳香胺、一氧化碳的氢氨羰基化反应，合成了系列四氢呋喃-3-甲酰胺类化合物。

同时考察了不同芳香胺作为底物的适应性，当苯胺上的取代基为烷基，卤素以及硝基时，均能得到四氢呋喃-3-甲酰胺类衍生物，收率为54.3%~93.2%。

用1h nmr、13c nmr对产物进行了结构表征。

2. 参考文献

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3. 毕业设计（论文）进程安排

2017.12.20 布置论文 2017.12.20-2017.12.30 查阅文献 2018.1.1-2018.1.13 撰写开题报告 2018.2.26-2018.3.3 实验准备工作 2018.3.6-2018.5.31 实验工作 2018.6.1-2018.6.5 撰写论文，准备答辩