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肟菌酯的合成工艺
引用本文:陆翠军,刘建华,杜晓华.肟菌酯的合成工艺[J].农药,2011,50(3).
作者姓名:陆翠军  刘建华  杜晓华
作者单位:浙江工业大学,催化加氢研究中心,杭州,310014
摘    要:方法]以苯酞为主要原料,先与双(三氯甲基)碳酸酯(BTC)开环反应生成邻氯甲基苯甲酰氯,再与氰化钠反应得到邻氯甲基苯甲酰氰,甲醇酯化,然后与甲氧基胺盐酸盐肟化,最后与间三氟甲基苯乙酮肟缩合得到肟菌酯。结果]合成路线5步总收率22%。结论]该工艺简单经济,条件温和,适合工业化生产。

关 键 词:杀菌剂  肟菌酯  邻羟甲基苯甲酸内酯  合成  

Synthesis of Trifloxystrobin
LU Cui-jun,LIU Jian-hua,DU Xiao-hua.Synthesis of Trifloxystrobin[J].Pesticides,2011,50(3).
Authors:LU Cui-jun  LIU Jian-hua  DU Xiao-hua
Affiliation:LU Cui-jun,LIU Jian-hua,DU Xiao-hua(Catalytic Hydrogenation Research Center,Zhejiang University of Technology,Hangzhou 310014,China)
Abstract:Methods] Trifloxystrobin was synthesized using phthalide as a main starting material,by the reactions of phthalide ring-opening with bis(trichloromethyl) carbonate to give o-chloromethylbenzoyl chloride,cyaniding to give o-chloromethylbenzoyl cyanide,esterifying with methanol,oximating with methoxyaminium chloride,and condensating with 3-(trifluoromethyl) acetopheneone oxime.Results] The total yield was 22% based on phthalide.Conclusions] This process is simple,warm and economical,which is suitable for i...
Keywords:fungicide  trifloxystrobin  phthalide  synthesis  
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