摘要
以邻甲基苯乙酸为起始原料,经过氧化、酯化、肟化及溴代反应,最后与间三氟甲基苯乙酮肟缩合制备了杀菌剂肟菌酯.每步的反应产物均通过1 H NMR确认,总收率为17%.本工艺路线采用廉价的起始原料降低了生产成本,反应条件温和且易于控制,各步收率较高,有进一步研究与应用价值.
Trifloxystrobin was synthesized with a new method which adopted 2-methyl phenylacetate as the starting material through partial oxidation, esterification, oximation, bromization and condensation finally with 3'-(trifluoromethyl) acetophenone oxime. The reaction products of each step were confirmed by 1H NMR. The total yield was about 17%. The process route uses inexpensive starting materials, and reaction conditions are mild and easy control with good yield of each step, which is worthy of further study.
出处
《化学研究》
CAS
2014年第1期16-19,共4页
Chemical Research
基金
河南省科技厅基础前沿项目(132300410238)
关键词
邻甲基苯乙酸
杀菌剂
肟菌酯
合成
2-methyl phenylacetate
fungicide
trifloxystrobin
synthesis