Abstract
A dimethoxy amide chalcone has been synthesized in a two-step reaction. First, an amine chalcone was synthesized by the reaction of 4′-aminoacetophenone and 2,5-dimethoxybenzaldehyde using 40% NaOH solution as a catalyst in ethanol, and then followed by amidation through the reaction of the formed chalcone and succinic anhydride. The structure of the target compound was established by FTIR, HR-MS,1H-and13C-NMR, and 2D-NMR spectral analysis.
Original language | English |
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Article number | M938 |
Journal | MolBank |
Volume | 2017 |
Issue number | 2 |
DOIs |
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Publication status | Published - Jun 2017 |
Keywords
- Amide chalcones
- Amino chalcones
- Succinic anhydride