Isolation and structural elucidation by nuclear magnetic resonance (1H NMR, 13C NMR, DEPT135, COSY and HSQC) of compound (E) -1,3,5-trimethoxy-2- (prop-1-enyl) benzene extracted from Piper patulum.
DOI:
https://doi.org/10.54495/Rev.Cientifica.v30i2.279Keywords:
phytochemistry, spectroscopy, secondary metabolites, phenylpropanoid, antioxidant.Abstract
Guatemala is a country of great biological diversity, which has led natural product researchers to obtain results of great interest and scientific relevance, mainly in pharmacological properties; However, the molecular structure, conformations, and configurations of many secondary metabolites responsible for these properties are unknown. In this research, the objective was to isolate and elucidate the structure of a phenylpropanoid obtained from in the leaves of Piper patulum. The isolation was carried out by liquid-liquid extractions and chromatographic techniques (Column Chromatography -CC-), obtaining .092 g. The elucidation was performed by mass spectroscopy, infrared spectroscopy -IR- and nuclear magnetic resonance experiments -NMR-, the data obtained indicates the corresponding (E) -1,3,5-trimethoxy-2- (prop-1-enyl) benzene. Subsequently, the phenylpropanoid presented antioxidant activity through the qualitative test with 2,2-diphenyl-1-picrylhydrazyl-DPPH
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