Naturally Abundance Vanillin as Starting Material to Synthesizing 4-(4-Hydroxy-3-methoxyphenyl)-6-methyl-3,4-dihydropyrimidin-2(1H)-one
Indonesia is the second biggest producer of natural vanillin. Traditionally it was isolated from the bean of vanilla (Vanilla planifolia Andrews). This paper reports on applying vanillin as starting material for synthesizing a biologically important chemical structure 3,4-dihydropyrimidinone. The re...
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doaj-7df1d8bef3da4b3fadbff5266f7d5a802020-11-24T23:12:54ZengUniversity of BrawijayaJournal of Pure and Applied Chemistry Research2302-46902015-12-01438893Naturally Abundance Vanillin as Starting Material to Synthesizing 4-(4-Hydroxy-3-methoxyphenyl)-6-methyl-3,4-dihydropyrimidin-2(1H)-oneMasruri MASRURI0Yuga Adi Pranata1Brawijaya UniversityBrawijaya UniversityIndonesia is the second biggest producer of natural vanillin. Traditionally it was isolated from the bean of vanilla (Vanilla planifolia Andrews). This paper reports on applying vanillin as starting material for synthesizing a biologically important chemical structure 3,4-dihydropyrimidinone. The reaction was undertaken in one step following multi component reaction (MCR). Products determination was undergone using FTIR and UV-Vis spectrophotometry, and also liquid chromatography-mass spectrometry (LCMS). After purification under flash column chromatography in ethyl acetate-hexane, it was found a white solid of 4-(4-hydroxy-3-methoxyphenyl)-6-methyl-3,4-dihydropyrimidin-2(1H)-one in 67% yield with a few amount of an unreacted vanillin.http://jpacr.ub.ac.id/index.php/jpacr/article/view/216/pdf_2vanillinVanilla planifoniaBiginellisecondary metabolitedihydropyrimidinone |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Masruri MASRURI Yuga Adi Pranata |
spellingShingle |
Masruri MASRURI Yuga Adi Pranata Naturally Abundance Vanillin as Starting Material to Synthesizing 4-(4-Hydroxy-3-methoxyphenyl)-6-methyl-3,4-dihydropyrimidin-2(1H)-one Journal of Pure and Applied Chemistry Research vanillin Vanilla planifonia Biginelli secondary metabolite dihydropyrimidinone |
author_facet |
Masruri MASRURI Yuga Adi Pranata |
author_sort |
Masruri MASRURI |
title |
Naturally Abundance Vanillin as Starting Material to Synthesizing 4-(4-Hydroxy-3-methoxyphenyl)-6-methyl-3,4-dihydropyrimidin-2(1H)-one |
title_short |
Naturally Abundance Vanillin as Starting Material to Synthesizing 4-(4-Hydroxy-3-methoxyphenyl)-6-methyl-3,4-dihydropyrimidin-2(1H)-one |
title_full |
Naturally Abundance Vanillin as Starting Material to Synthesizing 4-(4-Hydroxy-3-methoxyphenyl)-6-methyl-3,4-dihydropyrimidin-2(1H)-one |
title_fullStr |
Naturally Abundance Vanillin as Starting Material to Synthesizing 4-(4-Hydroxy-3-methoxyphenyl)-6-methyl-3,4-dihydropyrimidin-2(1H)-one |
title_full_unstemmed |
Naturally Abundance Vanillin as Starting Material to Synthesizing 4-(4-Hydroxy-3-methoxyphenyl)-6-methyl-3,4-dihydropyrimidin-2(1H)-one |
title_sort |
naturally abundance vanillin as starting material to synthesizing 4-(4-hydroxy-3-methoxyphenyl)-6-methyl-3,4-dihydropyrimidin-2(1h)-one |
publisher |
University of Brawijaya |
series |
Journal of Pure and Applied Chemistry Research |
issn |
2302-4690 |
publishDate |
2015-12-01 |
description |
Indonesia is the second biggest producer of natural vanillin. Traditionally it was isolated from the bean of vanilla (Vanilla planifolia Andrews). This paper reports on applying vanillin as starting material for synthesizing a biologically important chemical structure 3,4-dihydropyrimidinone. The reaction was undertaken in one step following multi component reaction (MCR). Products determination was undergone using FTIR and UV-Vis spectrophotometry, and also liquid chromatography-mass spectrometry (LCMS). After purification under flash column chromatography in ethyl acetate-hexane, it was found a white solid of 4-(4-hydroxy-3-methoxyphenyl)-6-methyl-3,4-dihydropyrimidin-2(1H)-one in 67% yield with a few amount of an unreacted vanillin. |
topic |
vanillin Vanilla planifonia Biginelli secondary metabolite dihydropyrimidinone |
url |
http://jpacr.ub.ac.id/index.php/jpacr/article/view/216/pdf_2 |
work_keys_str_mv |
AT masrurimasruri naturallyabundancevanillinasstartingmaterialtosynthesizing44hydroxy3methoxyphenyl6methyl34dihydropyrimidin21hone AT yugaadipranata naturallyabundancevanillinasstartingmaterialtosynthesizing44hydroxy3methoxyphenyl6methyl34dihydropyrimidin21hone |
_version_ |
1716349946648592384 |