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(Z)-7-苯亚甲基-5H-二苯并[b,g][1,4]氧氮杂环辛-6(7H)-酮的合成

Synthesis of (Z)-7-Benzylidene-5 H-dibenzo[b,g][1,4]oxazocin-6(7 H)-one
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摘要 以2-碘苯酚和2-氟硝基苯为原料,经Ullmann缩合、还原、Sonogashira偶联、羰基环化反应首次合成了(Z)-7-苯亚甲基-5 H-二苯并[b,g][1,4]氧氮杂环辛-6(7 H)-酮,总收率34.9%。产物结构经1 H NMR、13C NMR和MS表征。 The new compound (Z)-7-benzylidene-5H-dibenzo[b, g][-1, 4-]oxazocin-6(7H)-one was synthe- sized through Ullmann etherification, reduction, Sonogashira coupling and intramolecular earbonylation reaction using 2-iodophenol and 1-fluoro-2-nitrobenzene as raw materials. The total yield was 34.9%. The Product structure was characterized by 1H NMR, 13C NMR and GC-MS.
出处 《化学世界》 CAS CSCD 北大核心 2013年第11期679-681,688,704,共5页 Chemical World
基金 湖南省科技厅科技项目(2011FJ3125 2011FJ3248) 湖南省教育厅科研资助项目(09C229)
关键词 (Z)-7-苯亚甲基-5 H-二苯并[b g][1 4]氧氮杂环辛-6(7 H)-酮 分子内羰基化 合成 (Z)-7-benzylidene-5 H-dibenzo[-b, g-] [- 1, 4-] oxazocin-6 (7 H)-one intramolecular carbonylation synthesis
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参考文献12

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