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2-氨基-4-苯基噻唑的合成研究
引用本文:曾振芳,韦友欢,黄秋婵.2-氨基-4-苯基噻唑的合成研究[J].广东化工,2014(1):28-28,41.
作者姓名:曾振芳  韦友欢  黄秋婵
作者单位:广西民族师范学院化学与生物工程系,广西崇左532200
基金项目:广西民族师范学院科研基金资助项目(2012XYYB001);广西高校优秀人才资助计划(RC2007043)
摘    要:以α-溴代苯乙酮和硫脲为原料,正丙醇为溶剂,制得2-氨基-4-苯基噻唑,通过元素分析、红外光谱、1H NMR和MS确定化合物的结构。运用正交实验筛选出最佳工艺条件:反应时间为6 h,温度为97℃(回流),α-溴代苯乙酮和硫脲摩尔比为1:1.10,2-氨基-4-苯基噻唑的产率可达97%。该方法具有安全,易控制,操作简便,后处理简单等优点,适合工业化生产。

关 键 词:-氨基--苯基噻唑  合成  硫脲  正交实验

Study on Synthesis of 2-amino-4-phenylthiazole
Zeng Zhenfang,Wei Youhuan*,Huang Qiuchan.Study on Synthesis of 2-amino-4-phenylthiazole[J].Guangdong Chemical Industry,2014(1):28-28,41.
Authors:Zeng Zhenfang  Wei Youhuan*  Huang Qiuchan
Affiliation:(Department of Chemistry and Biological Engineering, Guangxi Normal University for Nationalities, Chongzuo 532200, China)
Abstract:In the paper, 2-amino-4-phenylthiazole was synthesized by reaction of α-bromoacetophenone and thiourea with 1-propanol as solvent, its structure has been determined by elemental analysis, IR, 1H NMR and MS. The optimum condition which was selected by orthogonal experiments is at 97 ℃(reflux) for 6 h, the ratio of α-bromoacetophenone and thiourea was 1:1.10(mol), and the yield reached 97 %. This method has the characteristics of safety, easy control and simple operation. It has valuable for industrial applied.
Keywords:2-amino-4-phenylthiazole  synthesis  thiourea  orthogonal experiments
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