摘要
[目的]硅噻菌胺是小麦全蚀病选择性防治药剂,然而该药剂的规模合成存在着很大挑战,为此,研究开发了硅噻菌胺的新合成工艺。[方法]该工艺以3-氯-2-丁酮、丙炔酸甲酯为起始原料,通过取代、环合、硅烷化和酰胺化等4步反应,方便地得到目的产物。[结果]该工艺具有原料易得、反应易控、反应媒介易于回收使用、单步收率高等特点。[结论]具有工业应用前景。
[Aims] Silthiopham was a selective fungicide for the control of take-all disease.However,its scale preparation faced big challenges.So,a new process was explored.[Methods] Silthiopham was afforded conveniently by using 3-chlorobutan-2-one and methyl propiolate as starting materials in four steps via substitution,cyclization,silylanization and amidation.[Results] The procedure showed several advantages such as easily available raw materials,mild reaction conditions,easily recycled reaction medium and high single-step yields.[Conclusions] It could be applied to industrial production.
出处
《农药》
CAS
CSCD
北大核心
2013年第7期484-486,共3页
Agrochemicals
关键词
硅噻菌胺
小麦全蚀病
成环反应
硅烷化
合成
silthiopham
take-all disease
cyclization reaction
silylanization
synthesis