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., & 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
Natiq G. Ahmad; Moayed J. Mohammed; Neam H. Saleem. "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
VANCOUVER
G. Ahmad, N., J. Mohammed, M., H. Saleem, N. Synthesis of Some Unsaturated Quinoline Derivatives. Kirkuk Journal of Science, 2018; 13(2): 177-184. doi: 10.32894/kujss.2018.145754
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