Abstract
1,3-Oxazole-5-one blends 2(a-c) have been set up by cyclization of compound (1) with aromatic aldehyde auxiliaries. The starting compound (1) was expeditiously procured by the reaction of 4-chlorobenzoylchloride with aminoacetic acid. Blends 2(a-c) were changed over into a grouping of subordinates by the reaction with ethylenediamine to masterminded 3(a-c) by then blends 3(a-c) reaction with aromatic aldehydes subsidiaries to organized 4(a-c). Each new compound was depicted by Proton atomic attractive reverberation (1H-NMR), Fourier changes infrared spectroscopy (FTIR), and Ultraviolet (UV) spectroscopy.
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