氟啶虫酰胺合成方法述评  

a Review of synthetic Methods of flonicamid

作　　者：刘鹏飞[1] 孙克[1] 张敏恒[1] 

机构地区：[1]沈阳化工研究院有限公司新农药创制与开发国家重点实验室,沈阳110021

出　　处：《农药》2013年第8期615-619,共5页Agrochemicals

基　　金：十二五”国家科技支撑计划项目(2011BAE06B00);国家重点基础研究计划(973计划)项目(2012CB724501)

摘　　要：总结了文献报道的氟啶虫酰胺及其中间体的合成工艺路线和具体的合成方法。氟啶虫酰胺是由4-三氟甲基烟酸为主要原料经过化学反应得到。主要有2条工艺路线。The synthetic method and detailed process of flonicamid and its intermediates reported in the literature were summarized. There were two main different process routes to synthesize flonicamid. It was prepared by several chemical reactions starting from 4-trifluoromethylnicotinic acid.

关 键 词：氟啶虫酰胺 工艺路线 合成方法 

分 类 号：TQ453.2[化学工程—农药化工]