Benosmane, N.Boutemeur, B.Hamdi, S.m.Hamdi, M.2020-10-282020-10-282016-09-01Articale in Journal of fundamental and Applied Sciences Vol. 08, N. 031112-9867http://dspace.univ-eloued.dz/handle/123456789/7347Articale in Journal of fundamental and Applied Sciences Vol. 08, N. 03A new series of 3,3'-{alkane-α,ω-diylbis[imino-eth-1-yl-1-ylidene]}bis(6-methyl-2H-pyran- 2,4(3H)-dione) derivatives (3c-e) has been synthesized by the convenient ultrasound-mediated condensation of a diamine with dehydroacetic acid in the presence of a catalytic amount of p- toluenesulfonic acid. The structure of all synthesized compounds was elucidated by IR spectroscopy, 1H NMR spectroscopic spectra, elemental analysis, and mass spectroscopy. A tautomeric form for the derivatives species is also proposed.enDehydroacetic acid; Schiff base; Condensation; Catalyst; Ultrasound irradiation; Tautomerism.A Convenient Synthesis Of Pyrandione Derivatives Using P-toluenesulfonic Acid As Catalyst Under Ultrasound IrradiationArticle