CAS: 207994-08-9; 5-Chloro-3-Fluoropicolinic Acid

该化合物是有机化合物,其特点是其丙烯环结构,这是一个六人组成的芳香环,含有一个氮原子;该化合物在环的2处有一个碳苯基酸功能组(COOH),有助于其酸性和反应性;氯和氟代金酸分别在5和3个位置的存在,带来独特的电子和消毒效应,可能影响化合物的化学行为和相互作用;通常,这种卤代丙烯衍生物具有更强的脂性,可作为合成药物或农用化学的中间体;该化合物在室温下很固,由于其结构特征可能被用于医药化学,其特性,如溶解性和稳定性,可因具体情况和其他功能组的存在而不同;在处理和使用时,应参考安全数据,因为卤代化合物具有不同程度的毒性.

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214055-12-6 207994-11-4 214055-11-5

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合成工艺路线路线简述

    📜2-溴-3-氟-5-氯吡啶置于正丁基锂,异丙基氯化镁体系中,用 四氢呋喃,正己烷,甲苯 用作溶剂,化学反应 4.0H,反应生成5-氯-3-氟-2-吡啶羧酸
    参考文献:Creating Structural Manifolds From A Common Precursor: Basicity Gradient-Driven Isomerization Of Halopyridines
    标题:Creating Structural Manifolds From A Common Precursor: Basicity Gradient-Driven Isomerization Of Halopyridines
    摘要:5-Chloro-2,3-Difluoropyridine,An Intermediate In The Manufacturing Process Of An Industrial Pesticide,Can Be Hydrolyzed To 5-Chloro-3-Fluoro-2H-Pyridinone And The Latter Converted Into 2,5-Dichloro-3-Fluoropyridine (1A),2-Bromo-5Chloro-3-Fluoropyridine (1B),5-Chloro-3-Fluoro-2-Iodopyridine (1C) And 3-Chloro-5-Fluoropyridine (1D). Consecutive Treatment Of These Four Substrates With Lithium Diisopropylamide And Carbon Dioxide Or Lithium Diisopropylamide And Iodine Affords The Corresponding 4-Pyridinecarboxylic Acids 2 And 4-Iodopyridines 3,Respectively. Amide-Promoted Deprotonation Of Such 4-Iodopyridines 3 Triggers An Isomerization In Which Lithium And Iodine Change Places. The Resulting Species Can Be Trapped With Carbon Dioxide To Give The Acids 5A-C Or Neutralized To Give The Halopyridines 4A-C. The Iodopyridines 4A And 4B Can Be Converted Into The Acids 6A And 6B,The Latter Product Leading Also To The Congeners 6C And 6D. The Diiodopyridine 4C Provides An Entry To The Halopyridine 4D,Which At The Same Time May Act As The Precursor To The Acid 5D,The Acid 7 Or The Bisacid 8. Finally,The Acid 9 Is Accessible From Either One Of The 5-Chloro-3-Fluoro-2-Halopyridines 1B And 1C. (C) Wiley-Vch Verlag Gmbh & Co. Kgaa,69451 Weinheim,Germany,2002).
    Doi:10.1002/1099-0690(200212)2002:24<4174::Aid-Ejoc4174>3.0.Co;2-6

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