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作 者:丁丽琴[1] 张群朝[1] 龙帅[1] 张爱清[1]
机构地区:[1]中南民族大学化学与材料科学学院湖北省催化与材料科学重点实验室,湖北武汉430074
出 处:《功能材料》2007年第5期856-858,共3页Journal of Functional Materials
基 金:国家自然科学基金资助项目(50373052)
摘 要:报道了由硝基苯甲醛和丙酮经Claisen-Schmidt缩合而制得1,5-二硝基苯基-1,4-戊二烯-3-酮,然后在SnCl2.2H2O-HCl还原体系下,得到1,5-二胺基苯基-1,4-戊二烯-3-酮,同时讨论了影响产率的几个因素。与文献报道相比,此方法具有反应条件温和、操作简便和收率高(91.7%)等优点。产物结构通过元素分析、熔点I、R和1H NMR证实。1, 5-dinitroaryl-1,4-pentadien-3-ones were synthesized by the Claisen-Schmidt condensation of nitrobenzaldehyde and acetone. Then reduction of 1,5-dinitroaryl-1,4-pentadien-3-ones to the corresponding diamines were performed in hydrochloric acid using stannous chloride as reduction agent. The factors influencing the product yields were also discussed. Compared with previous methods in the literature, the present procedure has the advantages of milder conditions, lower cost, easier work-up, high product yield (91.7 %). The products were characterized by elemental analysis, melting points, IR, and 1 H NMR measurements.
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