SHORT COMMUNICATIONS
Unexpected Formation of Bis(hydrazinecarboximidamide) via Ultrasound Promoted Rearrangement of Epoxy Ketone
Published 2017-07-02
Keywords
- α,β-epoxy ketones,
- pyrazoles,
- ultrasound,
- unexpected reaction
How to Cite
(1)
Brasil, S. R.; Capiotto, A. do C.; Flores, A. F. C.; Back, D. F.; Faoro, E.; Pizzuti, L. Unexpected Formation of Bis(hydrazinecarboximidamide) via Ultrasound Promoted Rearrangement of Epoxy Ketone. Orbital: Electron. J. Chem. 2017, 9 (3), 204-209.
Abstract
An efficient synthesis of aromatic pyrazoles via cyclocondensation of epoxy chalcones with hydrazine is reported. When aminoguanidine hydrochloride is the dinucleophilic specie the reaction leads to a mixture of amidino pyrazole and a minor amount (15%) of an interesting co-product identified as 2,2'-(1,3-diphenylpropane-1,2-diylidene)bis(hydrazinecarboximidamide) dihydrochloride by X-ray diffraction and NMR. A plausible mechanism for the co-product formation via rearrangement of the epoxy chalcone into 1,2-diketone followed by the condensation with aminoguanidine reaction is proposed.
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