Dibenzyl acetone was prepared from the reaction of one mole acetone with two moles of benzaldehyde in the presence of sodium hydroxide as a base. A number of quinoline were prepared by refluxing the dibenzyl acetone with aniline and its derivatives (o, m, and p-nitoaniline; m, and p-hydroxyaniline; p-chloroaniline and p-toluidine).
The structures of the prepared compounds were assigned according to elemental analyses results as well as UV-visible and IR spectra.
G. Ahmad,N , J. Mohammed,M and H. Saleem,N . (2018). Synthesis of Some Unsaturated Quinoline Derivatives. Kirkuk Journal of Science, 13(2), 177-184. doi: 10.32894/kujss.2018.145754
MLA
G. Ahmad,N , , J. Mohammed,M , and H. Saleem,N . "Synthesis of Some Unsaturated Quinoline Derivatives", Kirkuk Journal of Science, 13, 2, 2018, 177-184. doi: 10.32894/kujss.2018.145754
HARVARD
G. Ahmad N, J. Mohammed M, H. Saleem N. (2018). 'Synthesis of Some Unsaturated Quinoline Derivatives', Kirkuk Journal of Science, 13(2), pp. 177-184. doi: 10.32894/kujss.2018.145754
CHICAGO
N G. Ahmad, M J. Mohammed and N H. Saleem, "Synthesis of Some Unsaturated Quinoline Derivatives," Kirkuk Journal of Science, 13 2 (2018): 177-184, doi: 10.32894/kujss.2018.145754
VANCOUVER
G. Ahmad N, J. Mohammed M, H. Saleem N. Synthesis of Some Unsaturated Quinoline Derivatives. Kirkuk J. Sci.. 2018;13(2):177-184. doi: 10.32894/kujss.2018.145754
