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5-(2,3-二氯苯氧基)-4-氯-2-硝基苯胺合成工艺的研究
引用本文:崔志芹,王志祥.5-(2,3-二氯苯氧基)-4-氯-2-硝基苯胺合成工艺的研究[J].化工时刊,2006,20(8):24-26.
作者姓名:崔志芹  王志祥
作者单位:中国药科大学药学院,江苏,南京,210009
摘    要:研究了以2,3-二氯苯酚和4,5-二氯-2-硝基苯胺通过缩合反应制备5-(2,3-二氯苯氧基)-4-氯-2-硝基苯胺的合成工艺。着重考察了催化剂、反应时间、加料速率、加料顺序等因素对缩合反应的影响。结果表明,不同催化剂对反应选择性的影响很大,采用适宜的催化剂可有效抑制副反应的发生,选择性可达95%。转化率随时间的延长而逐渐增加,反应选择性随时间的延长慢慢下降,反应时间宜控制在8 h左右,收率可达88%。

关 键 词:2  3-二氯苯酚4  5-二氯-2-硝基苯胺三氯苯哒唑
收稿时间:2006-05-31
修稿时间:2006年5月31日

Synthesis conditions for 5-(2,3-dichlorophenoxy)-4-chloro-2-nitrobenzenamine
Cui Zhiqin,Wang Zhixiang.Synthesis conditions for 5-(2,3-dichlorophenoxy)-4-chloro-2-nitrobenzenamine[J].Chemical Industry Times,2006,20(8):24-26.
Authors:Cui Zhiqin  Wang Zhixiang
Affiliation:College of Pharmaceutics, China Pharmaceutical University, Jiangsu Nanjing 210009
Abstract:5-(2,3-dichlorophenoxy)-4-chloro-2-nitrobenzenamine,an important intermediate of triclabendazole was synthesized by using 2,3-dichlorophenol and 4,5-dichloro-2-nitrobenzenamine.Influences of catalysts,reaction time,the sequence and velocity of adding materials were observed.Selectivity was significant affected by the kind of catalysts.Selectivity was 95% if the suitable catalyst was used.The conversion rate increased and selectivity decreased with time going on.Yield reached 88% when reaction time was 8 hours and decreased after that.The by-reaction increased in alkaline environment.
Keywords:2  3-dichlorophenol 4  5-dichloro-2-nitrobenzenamine triclabendazole
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