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6-氰基吲哚-3-甲醛的合成

Synthesis of 6-Cyanoindole-3-carboxaldehyde

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【作者】 葛裕华吴亚明薛忠俊

【Author】 GE Yu-Hua~*, WU Ya-Ming, XUE Zhong-Jun(Department of Chemistry & Chemical Engineering,Southeast University,Nanjing 210096)

【机构】 东南大学化学化工系东南大学化学化工系 南京210096南京210096南京210096

【Abstract】 Intermediate 6-cyanoindole was obtained from 4-methylbenzonitrile as a raw material via nitration with the mixed acid, condensation with N,N-dimethylformamide dimethyl acetal and cyclic reaction with Raney nickel-hydrazine. 6-Cyanoindole-3-carboxyaldehyde was synthesized via the Vilsmeier reaction of 6-(cyanoindole) with N,N-(diemthylformamide) and phosphorus oxychloride. The structure of the target compound was confirmed by 1H NMR, IR and elemental analysis. The total yield was 57% and the purity of the final (product) reached 99.4%.

【关键词】 氰基吲哚氰基吲哚甲醛合成
【Key words】 cyanoindolecyanoindolecarboxaldehydesynthesis
  • 【文献出处】 应用化学 ,Chinese Journal of Applied Chemistry , 编辑部邮箱 ,2005年04期
  • 【分类号】O626
  • 【被引频次】8
  • 【下载频次】453
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