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N-氨基咔唑合成的研究

Synthesis of N-am ino-carbazole

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【作者】 崔慧玲王丽红白官李笃信林培华

【Author】 CUIHui-ling,WANG Li-hong,BAIGuan,LIDu-xin,LIN Pei-hua(School of Chem istry and Chem ical Engineering,Shanxi University,Taiyuan 030006,China)

【机构】 山西大学化学化工学院山西大学化学化工学院 山西太原030006山西太原030006

【摘要】 以咔唑为起始原料,经亚硝化和还原两步反应合成N-氨基咔唑。在亚硝化反应中,采用二甲基亚砜为溶剂,咔唑与亚硝酸钠反应的摩尔比为2.4∶5.8,反应最佳温度为27~30℃,反应时间为2 h,产率为86%。在还原反应中采用无水乙醇和冰醋酸的混和溶剂,两种溶剂的体积比为2∶1,以锌粉为还原剂,反应温度为25~35℃,反应时间为2 h,产率为81%。目的物及中间体经IR、1H NMR及元素分析测试,证明其结构是正确的,同时对产物的荧光性质进行了初步研究。

【Abstract】 A new synthesis method ofN-am ino-carbazole was stud ied in this article.Itwas synthesized on the basis of carbazole by two steps reaction of nitrosation and reduction.The DMSO was used as solvent in nitrosation reaction,which the mole ratio of carbazole to NaNO2was 2.4∶5.8,reacted for 2 h at 27 ~ 30℃,the yield was 86%.Anhydrous alcohol and glacial acetic acid were used as component solvent,which the volume ratio was 2∶1,zinc dust as reductant,reaction temperature was 25~35℃,reaction time was 2 h,the yield was 81%.The structures of object compound and intermed iate were identified by IR,1H NMR and elementary analysis.And their fluorescence characteristic were researched.

【关键词】 N-氨基咔唑咔唑合成
【Key words】 N-am ino-carbazolecarbazolesynthesis
  • 【文献出处】 应用化工 ,Applied Chemical Industry , 编辑部邮箱 ,2006年04期
  • 【分类号】O626.2
  • 【被引频次】9
  • 【下载频次】473
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