V–Mg–O catalysts for oxidative dehydrogenation of alkylpyridines and alkylthiophenes

Vanadium appears to be the element that is most frequent (along with molybdenum) used in the catalyst formulations for oxidative dehydrogenation (ODH) of hydrocarbons and alcohols. In the present work the employment of ODH reaction in the presence of air has been extended for the preparation of vinyl substituted pyridines and thiophenes using vanadium (and for comparison molybdenum) oxide catalysts. The efficiency of vanadium–magnesium oxide catalysts in the production of vinylpyridines and vinylthiophenes has been evaluated. A strong dependence of the yield and selectivity of the latter upon the vanadium (molybdenum) oxide loading and the conditions of heat treatment were observed. In optimized reaction conditions V–Mg–O catalysts at the temperature approximate 450 °C ensured the formation of vinylpyridines and vinylthiophenes with the yield of 40–60% at the selectivity of 90%. In prolonged runs no visible changes in the performance of the catalyst were observed. DTA–DTG, XRD, IR ESR, NMR methods have been used detecting the formation of species of V–Mg–O catalysts that appear to be responsible for the catalyst efficiency in the reactions under consideration.