Reichel Marco, Sile Sami, Kornath Andreas, Karaghiosoff Konstantin
Department of Chemistry, Ludwig-Maximilian University Munich, Butenandtstrasse 5-13 (D), 81377 Munich, Germany.
School of Natural and Environmental Sciences, Agriculture Building, King's Road, Newcastle upon Tyne NE1 7RU, U.K.
J Org Chem. 2021 Mar 19;86(6):4423-4431. doi: 10.1021/acs.joc.0c02670. Epub 2021 Mar 4.
Fluoromethyl-2,4,6-trinitrophenylsulfonate has been prepared for the first time and qualified as a simple to use monofluoromethylating reagent. Its molecular structure in the solid state has been determined by single-crystal X-ray diffraction studies. This reagent proves to be effective for the electrophilic introduction of a CHF group into selected chalcogen and nitrogen nucleophiles. Monofluoromethyl derivatives of various bifunctional N,O-nucleophiles have been synthesized using fluoromethyl-2,4,6-trinitrophenylsulfonate. Due to the good crystallizing properties of the anion, the fluoromethylated products as well as side products that are difficult to identify by nuclear magnetic resonance spectroscopy can readily be characterized by X-ray crystallographic techniques.
首次制备了氟甲基 - 2,4,6 - 三硝基苯磺酸酯,并将其鉴定为一种易于使用的单氟甲基化试剂。通过单晶X射线衍射研究确定了其固态分子结构。该试剂被证明可有效地将CHF基团亲电引入选定的硫属元素和氮亲核试剂中。使用氟甲基 - 2,4,6 - 三硝基苯磺酸酯合成了各种双功能N,O - 亲核试剂的单氟甲基衍生物。由于阴离子具有良好的结晶性能,通过X射线晶体学技术可以很容易地对氟甲基化产物以及难以通过核磁共振光谱鉴定的副产物进行表征。