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1,1’-二茂铁二羧酸二辛酯的合成方法研究

Research on Synthesis Methods of Dioctyl 1,1’-Ferrocenedicarboxylate

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【作者】 何宜丰聂教荣俞艳李慧李晓强杨军

【Author】 HE Yifeng1,NIE Jiaorong1,YU Yan2,LI Hui2,LI Xiaoqiang2,YANG Jun2(1.The State Owned Jianghe Chemical Factory,Yuan’an 444200,China;2.Shanghai Institute of Organic Chemistry,CAS,Shanghai 200032,China)

【机构】 国营江河化工厂中国科学院上海有机化学研究所

【摘要】 对1,1’-二茂铁二羧酸二辛酯的合成方法开展了研究。通过二茂铁的Friedel-Crafts酰基化反应合成了1,1’-二乙酰基二茂铁,然后用次氯酸钠氧化1,1’-二乙酰基二茂铁得到1,1’-二茂铁二甲酸。研究了1,1’-二茂铁二甲酸直接酯化法制备1,1’-二茂铁二甲酸二甲酯,以其为原料通过酯交换的方法可以65%的收率和四步合计48%的总收率实现1,1’-二茂铁二甲酸二辛酯的合成,产物结构用1H-NMR、IR进行了表征。

【Abstract】 The synthesis methods of dioctyl 1,1’-ferrocenedicarboxylate were studied.The 1,1’-diacetyl ferrocene was synthesized by Friedel-Crafts acylation reaction of ferrocene.The 1,1’-ferrocenedicarboxylic acid was prepared by subsequent oxidation of the obtained 1,1’-diacetyl ferrocene with sodium hypochlorite.The preparation process of dimethyl 1,1’-ferrocenedicarboxylate by using direct esterification method of 1,1’-ferrocenedicarboxylic acid was studied.Using dimethyl 1,1’-ferrocenedicarboxylate as raw material,the synthesis of dioctyl 1,1’-ferrocenedicarboxylate by transesterification method can be realized with 65% yield and 48% total yield during four steps.The product structure was characterized by using 1H-NMR and IR.

【基金】 国家自然科学基金资助(批准号:20802088,91017006,90917017)
  • 【文献出处】 化学推进剂与高分子材料 ,Chemical Propellants & Polymeric Materials , 编辑部邮箱 ,2012年06期
  • 【分类号】O627.81
  • 【被引频次】1
  • 【下载频次】280
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