第 35 卷第 3 期Vol. 35 No. 3
2005 年 6 月Jun 2005

所属栏目:其它

1-溴-5-苯基-四氮唑的合成
魏先红; 何宝娟; 陈泳洲(湖北师范学院化学与环境工程系; 湖北黄石)
摘 要:以苯甲腈、叠氮钠、溴等为原料,经偶合,溴化合成了1-溴-5-苯基四氮唑。研究了反应时间、反应温度、溶剂与反应物配比对产品收率的影响。实验表明:在n(苯甲腈)∶n(叠氮钠)=1∶1.1,1 mol NH4Cl催化,120℃下反应20 h可得到收率90%的5-苯基四氮唑。在n(5-苯基四氮唑)∶n(溴)∶n(氢氧化钠)=1∶0.97∶0.96,反应4 h,水作溶剂的条件下,可得到56.4%的1-溴-5-苯基四氮唑,两步反应后的总收率为49.1%。
关键词:1-溴-5-苯基-四氮唑; 5-苯基-四氮唑; 合成
中图分类号:O626.28  文献标识码:A  文章编号:1009-9212(2005)03-0011-02
Synthesis 1-Bromine -5-Phenyl-Tetrazole
WEI Xian-hong; HE Bao-juan; CHEN Yong-zhou(Hubei Normal University; Huangshi 435002; China)
Abstract:The product 1-Bromine -5-phenyl-tetrazole was synthesized from benzonitrile,Br_(2) and sodium azide by cyclization and bromization. The factors influencing the synthesis were discussed and the best reaction conditions were found out. The optimum conditions were as follow: molar ratio of benzonitrile to sodium azide was 1∶1.1, the catalyst adding was 1.0 mol NH_(4)Cl, the reaction temperature was 120 ℃, and reaction time was 20h, the yield of 5Phenyl-Tetrazole reached 90%; Molar ratio of 5-Phenyl-Tetrazole t...
Key words:1-bromine- 5-phenyl-tetrazole; 5-phenyl-tetrazole; Synthesis
收稿日期:2004-12-03
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