Abstract
2-Fluorinated thiocyanate compounds have been prepared by action of KSCN on an homologous series of 2-fluorotosylates in ethanol at about 100°C. The isomerization giving isothiocyanic derivatives does not take place under these conditions. The analysis of the NMR spectra on three members of the series has shown that the mechanism is of the SN 2 type.
Published Version
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