有机化学 2006, 26(04) 563-567  DOI:      ISSN: 0253-2786 CN: 31-1321/O6

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本文关键词相关文章
取代吲哚-3-甲醛
合成
Vilsmeier-Hacck反应
本文作者相关文章
葛裕华
葛裕华
葛裕华
吴亚明
吴亚明
吴亚明
薛忠俊
薛忠俊
薛忠俊
PubMed
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取代吲哚-3-甲醛类化合物的合成
葛裕华*,吴亚明,薛忠俊
(Department of Chemistry and Chemical Engineering, Southeast University, Nanjing 210096)
摘要: 取代邻硝基甲苯(1)、N,N-二甲基甲酰胺二甲基缩醛或二乙基缩醛和哌啶在溶剂N,N-二甲基甲酰胺中缩合制得取代的β-哌啶基-2-硝基甲苯(2), 2用铁粉和冰醋酸还原环合得到取代吲哚(3), 将3与三氯氧磷和N,N-二甲基甲酰胺通过Vilsmeier-Hacck反应制得了取代吲哚-3-甲醛类化合物45. 化合物45的结构经元素分析, IR和1H NMR确认.
关键词 取代吲哚-3-甲醛   合成   Vilsmeier-Hacck反应   
Synthesis of Substituted Indole-3-carboxaldehyde Derivatives
GE Yu-Hua*,WU Ya-Ming,XUE Zhong-Jun
Abstract: Substituted 2-nitro-β-piperidinostyrenes (2), obtained from the reaction of substituted 2-nitrotoluene (1), N,N-dimethylformamide dimethyl acetal or N,N-dimethylformamide diethyl acetal and piperidine in solvent of N,N-dimethylformamide, reacted with iron and acetic acid to yield the substituted indoles 3. Substituted indole-3-carboxaldehydes 4 and 5 were synthesized from 3 by Vilsmeier-Hacck reaction with phosphorus oxychloride and N,N-dimethylformamide. The structures of 4 and 5 were analyzed and established by elemental analysis, IR and 1H NMR spectra.
Keywords: substituted indole-3-carboxaldehyde   synthesis   Vilsmeier-Hacck reaction   
收稿日期 2005-06-08 修回日期 2005-10-31 网络版发布日期  
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