1871-73-4Relevant articles and documents
Bromofluorination of alkenes: 1-bromo-2-fluoro-2-phenylpropane [ Benzene, (2-bromo-1-fluoro-1-methylethyl ]
Haufe, Günter,Alvernhe, Gerard,Laurent, André,Ernet, Thomas,Goj, Olav,Kr?ger, Stefan,Sattler, Andreas
, p. 159 - 159 (2017/09/20)
-
A Rapid and Efficient Method for the Fluoroalkylation of Amines and Amides. Development of a Method Suitable for Incorporation of the Short-Lived Positron Emitting Radionuclide Fluorine-18
Chi, Dae Yoon,Kilbourn, Michael R.,Katzenellenbogen, John A.,Welch, Michael J.
, p. 658 - 664 (2007/10/02)
We have described a two-step method for the preparation of fluoroalkyl-substituted amines and amides.The sequence involves fluoride ion displacement of a haloalkyl trifluoromethanesulfonate (triflate), followed by fluoroalkylation of the heteroatom system (amine or amide) by the fluoroalkyl halide.Alternatively, the fluoroalkyl halide can be prepared by halofluorination of a terminal olefin.These reactions have been used to prepare various fluoroalkyl derivatives of N-phenylpiperazine and N-fluoroalkyl derivatives of the neuroleptic agent spiperone (7).The sequence is rapid, convenient, and efficient, even when fluoride ion is the limiting reagent.Therefore, it is readily adaptable to the preparation of a variety of compounds labeled with the short half-life (t1/2 = 110 min) positron-emitting radionuclide fluorine-18.
