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2-氨基-5-硝基苯酚的合成

Synthesis of 2-Amino-5-nitrophenol

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【作者】 李燕芸尹振晏胡应喜刘霞金振国

【Author】 LI Yan yun,YIN Zhen yan,HU Ying xi,LIU Xia,JIN Zhen guo (Department of Chemical Engineering,Beijing Institute of Potro Chemical Technology,Beijing 102600,China)

【机构】 北京石油化工学院化工系!北京102600

【摘要】 以邻氨基苯酚和尿素为原料 ,对环合、硝化、碱性水解的传统工艺进行改进 ,合成了 2 氨基 5 硝基苯酚。研究了影响环合反应的因素 ,优化了反应条件 ,总收率为 80 0 %。最优反应条件为 :n (邻氨基苯酚 )∶n (尿素 ) =1 0 0∶1 0 5 ,于 115℃反应 5 5h ,再硝化、碱性水解得产品。对三步的产品进行了红外光谱分析。传统工艺的收率仅为 36 %~ 5 3% ,三废量大。邻氨基苯酚 -尿素法 ,工艺新颖 ,原料易得、成本低 ,“三废”少。

【Abstract】 Amino 5 nitrophenol was synthesized using o aminophenol and urea as raw materials through cyclocondensation,nitration and alkaline hydrolysis in turn.Factors influencing the reactions were studied.The overall yield was 80%.The optimum conditions are as follows.In cyclocondensation, o aminophenol and urea (molar ratio 1.00∶1.05) reacted at 115 ℃ for 1.5 h.Nitration was carried out at 40 ℃ for 2 h with HNO\-3 and H\-2SO\-4,and alkaline hydrolysis at 105 ℃ for 2.5 h.The product was characterized by IR.This new method, o aminophenol urea method,is facile,of low cost and lacking in wastes.The overall yield of conventional process is only 36%-53%.

【关键词】 环合硝化碱性水解邻氨基苯酚
【Key words】 cyclocondensationnitrationalkaline hydrolysiso-aminophenol
  • 【分类号】TQ612.1;TQ24
  • 【被引频次】6
  • 【下载频次】429
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