当前位置: 首页 > 文章 > 高效氟吡甲禾灵的合成 现代农药 2009 (6) 25-27
Position: Home > Articles > Synthesis of R-(+)-Haloxyfop-methyl Modern Agrochemicals 2009 (6) 25-27

高效氟吡甲禾灵的合成

作  者:
徐强;王述刚;刘奎涛
单  位:
红太阳集团股份有限公司
关键词:
2-(4-羟基苯氧基)-3-氯-5-三氟甲基吡啶;高效氟吡甲禾灵;2,3-二氯-5-三氟甲基吡啶;除草剂;合成
摘  要:
研究了以对苯二酚及2,3-二氯-5-三氟甲基吡啶为原料,碳酸钾为缚酸剂,合成得到2-(4-羟基苯氧基)-3-氯-5-三氟甲基吡啶,再与S-2-氯丙酸甲酯合成得到高效氟吡甲禾灵。讨论了溶剂、反应时间、反应温度对合成高效氟吡甲禾灵的影响。结果表明,以N,N-二甲基乙酰胺为溶剂,碳酸钾为缚酸剂,在65℃下反应12h,高效氟吡甲禾灵的收率可以达到95.6%,光学纯度可以达到97.5%。此方法收率高,光学纯度好,具有工业化意义。
译  名:
Synthesis of R-(+)-Haloxyfop-methyl
作  者:
XU Qiang, WANG Shu-gang, LIU Kui-tao (Red Sun Group Co., Ltd., Nanjing 211300, China)
关键词:
2-(4-hydroxyphenoxy)-3-chloro-5-trifluoromethylpyridine; R-(+)-haloxyfop-methyl; 2,3-dichlor-5-trifluoro-methylpyridine; herbicides; synthesis
摘  要:
2-(4-Hydroxyphenoxy)-3-chloro-5-trifluoromethylpyridine was synthesized by monoetherification of hydroquinone with 2,3-dichlor-5-trifluoromethylpyridine. R-(+)-haloxyfop-methyl was prepared through the etherifying between 2-(4-hydroxyphenoxy)-3-chloro-5-trifluoromethylpyridine and S-(-)-methyl 2-chloropropionate. The influences of solvent, reaction time and reaction temperature on the production yield were investigated. Suitable reaction parameters for the synthesis were obtained as follows: solvent was DMAC; potassium carbonate was acid-binding agent; the mixture was reacted for 12 h at 65℃. The yield was 95.6%, and the optical purity was 97.5%.
计量
文章访问数: 6
HTML全文浏览量: 0
PDF下载量: 0

所属期刊