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微波辐射合成4(3H)-喹唑酮
引用本文:赵虹,周国平,曾楚怡.微波辐射合成4(3H)-喹唑酮[J].精细化工,2003,20(12):763-765.
作者姓名:赵虹  周国平  曾楚怡
作者单位:湘潭大学,化工系,湖南,湘潭,411105
摘    要:以邻氨基苯甲酸和甲酰胺为原料,在无溶剂条件下采用微波辐射法合成4(3H) 喹唑酮。实验结果表明:n(甲酰胺)/n(邻氨基苯甲酸)=10,反应物加热预混合,甲酰胺分批加料,微波辐射强度为180W,微波辐射时间为6~8min时,邻氨基苯甲酸的转化率可达96%以上,4(3H) 喹唑酮的收率在94%以上,反应速率比常规加热条件下提高45倍。

关 键 词:微波辐射  4(3H)-喹唑酮
文章编号:1003-5214(2003)12-0763-03

Synthesis of 4(3H)-Quinazolinone under Microwave Irradiation
ZHAO Hong,ZHOU Guo-ping,ZENG Chu-yi.Synthesis of 4(3H)-Quinazolinone under Microwave Irradiation[J].Fine Chemicals,2003,20(12):763-765.
Authors:ZHAO Hong  ZHOU Guo-ping  ZENG Chu-yi
Abstract:Using o-aminobenzoic acid and formamide as raw materials,4(3H)-quinazolinone was synthesized without solvent under microwave irradiation and normal pressure.The results showed that the optimal reaction conditions were that,the mole ratio of formamide to o-aminobenzoic acid was 10,and microwave irradiation time was 8 min with the power of 180 W;before the reaction all o-aminobenzoic acid and a quarter of total mass of formamide were mixed at 60 ℃,then the remainder of formamide was added intermittently during the reaction.The conversation of o-aminobenzoic acid reached 96% and the total yield of 4(3H)-quinazolinone was above 94%.The reaction rate was increased by 45 times against ordinary heating.
Keywords:microwave radiatation  4(3H)-quinazolinone
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