对甲苯磺酸四氟丙酯置于sodium Iodide体系中,用 二乙二醇 作为反应溶剂,170.0 °C,101.32 Kpa 条件下,反应生成 2,2,3,3-四氟碘代丙烷
参考文献:Highly Stereoselective Approach To 3-Fluoroalkylated (E)-Hex-3-Ene-1,5-Diyne Derivatives Via An Addition-elimination Reaction
标题:Highly Stereoselective Approach To 3-Fluoroalkylated (E)-Hex-3-Ene-1,5-Diyne Derivatives Via An Addition-elimination Reaction
摘要:Palladium(0)-Catalyzed Sonogashira Cross-Coupling Reaction Of 2-Fluoroalkylated (Z)-2-Fluoro-1-Iodoethene,Which Is Easily Prepared From Commercially Available Polyfluorinated Alcohols In Facile Three Steps,With Terminal Alkynes In Dmf At Room Temperature For 24 H Took Place Stereospeciflcally To Give The Corresponding 1-Fluoroalkylated (Z)-1-Fluorobut-1-En-3-Yne Derivatives In Good To Excellent Yield. Thus Obtained Fluoroalkylated 1-Fluoroenynes Were Effectively Subjected To Addition Elimination Reaction With Various Alkynyllithiums At Room Temperature,Leading To 3-Fluoroalkylated Hex-3-Ene-1,5-Diyne Derivatives In Good To High Yields With An Excellent E Selectivity. (C) 2013 Elsevier B.V. All Rights Reserved.
DOI:10.1016/j.Jfluchem.2013.09.010