Synthesis and Antioxidant Properties of Two New Derivatives of Indeno-Benzofuran
Ninhydrin reacts with poly-phenols in different ratios to produce tetracyclic adducts. Here, pyrogallol was used as a polyphenol compound. In the company of acidic ionic liquid (AIL), there was a selective reaction between the ortho-site of polyphenol and the ninhydrin’s carbonyl group. Mono-adduct...
Main Authors: | , , |
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Format: | Article |
Language: | English |
Published: |
Islamic Azad University
2020-02-01
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Series: | Journal of Chemical Health Risks |
Subjects: | |
Online Access: | http://www.jchr.org/article_671485_789240cead5fb3f0923fde1ace4c3906.pdf |
Summary: | Ninhydrin reacts with poly-phenols in different ratios to produce tetracyclic adducts. Here, pyrogallol was used as a polyphenol compound. In the company of acidic ionic liquid (AIL), there was a selective reaction between the ortho-site of polyphenol and the ninhydrin’s carbonyl group. Mono-adduct (1:1) 3 and bis-adduct (2:1) 4 were prepared as a solvent and a catalyst for the reaction of ninhydrin with pyrogallol in 1-(carboxymethyl)-3-methyl-1<em>H</em>-imidazolium chloride (mcmimCl). Purity of the products was approved by <sup>1</sup>H NMR,<sup> 13</sup>C NMR, IR and Mass Spectroscopy. Moreover, the antioxidant activity of novel derivatives investigated in this paper by 2, 2-diphenyl-1-picrylhydrazyl (DPPH) radical assay and butylated hydroxytoluene (BHT) was considered to be standard. The results indicated that mono-adduct showed the strongest antioxidant activity (IC50 = 5.289µg/ml). |
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ISSN: | 2251-6719 2251-6727 |