Cargando…
Enzymatic Synthesis of Fatty Hydroxamic Acid Derivatives Based on Palm Kernel Oil
Fatty hydroxamic acid derivatives were synthesized using Lipozyme TL IM catalyst at biphasic medium as the palm kernel oil was dissolved in hexane and hydroxylamine derivatives were dissolved in water: (1) N-methyl fatty hydroxamic acids (MFHAs); (2) N-isopropyl fatty hydroxamic acids (IPFHAs) and (...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264264/ https://www.ncbi.nlm.nih.gov/pubmed/25134767 http://dx.doi.org/10.3390/molecules16086634 |
_version_ | 1783375456545800192 |
---|---|
author | Jahangirian, Hossein Haron, Md Jelas Yusof, Nor Azah Silong, Sidik Kassim, Anuar Rafiee-Moghaddam, Roshanak Peyda, Mazyar Gharayebi, Yadollah |
author_facet | Jahangirian, Hossein Haron, Md Jelas Yusof, Nor Azah Silong, Sidik Kassim, Anuar Rafiee-Moghaddam, Roshanak Peyda, Mazyar Gharayebi, Yadollah |
author_sort | Jahangirian, Hossein |
collection | PubMed |
description | Fatty hydroxamic acid derivatives were synthesized using Lipozyme TL IM catalyst at biphasic medium as the palm kernel oil was dissolved in hexane and hydroxylamine derivatives were dissolved in water: (1) N-methyl fatty hydroxamic acids (MFHAs); (2) N-isopropyl fatty hydroxamic acids (IPFHAs) and (3) N-benzyl fatty hydroxamic acids (BFHAs) were synthesized by reaction of palm kernel oil and N-methyl hydroxylamine (N-MHA), N-isopropyl hydroxylamine (N-IPHA) and N-benzyl hydroxylamine (N-BHA), respectively. Finally, after separation the products were characterized by color testing, elemental analysis, FT-IR and (1)H-NMR spectroscopy. For achieving the highest conversion percentage of product the optimum molar ratio of reactants was obtained by changing the ratio of reactants while other reaction parameters were kept constant. For synthesis of MFHAs the optimum mol ratio of N-MHA/palm kernel oil = 6/1 and the highest conversion was 77.8%, for synthesis of IPFHAs the optimum mol ratio of N-IPHA/palm kernel oil = 7/1 and the highest conversion was 65.4% and for synthesis of BFHAs the optimum mol ratio of N-BHA/palm kernel oil = 7/1 and the highest conversion was 61.7%. |
format | Online Article Text |
id | pubmed-6264264 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-62642642018-12-10 Enzymatic Synthesis of Fatty Hydroxamic Acid Derivatives Based on Palm Kernel Oil Jahangirian, Hossein Haron, Md Jelas Yusof, Nor Azah Silong, Sidik Kassim, Anuar Rafiee-Moghaddam, Roshanak Peyda, Mazyar Gharayebi, Yadollah Molecules Article Fatty hydroxamic acid derivatives were synthesized using Lipozyme TL IM catalyst at biphasic medium as the palm kernel oil was dissolved in hexane and hydroxylamine derivatives were dissolved in water: (1) N-methyl fatty hydroxamic acids (MFHAs); (2) N-isopropyl fatty hydroxamic acids (IPFHAs) and (3) N-benzyl fatty hydroxamic acids (BFHAs) were synthesized by reaction of palm kernel oil and N-methyl hydroxylamine (N-MHA), N-isopropyl hydroxylamine (N-IPHA) and N-benzyl hydroxylamine (N-BHA), respectively. Finally, after separation the products were characterized by color testing, elemental analysis, FT-IR and (1)H-NMR spectroscopy. For achieving the highest conversion percentage of product the optimum molar ratio of reactants was obtained by changing the ratio of reactants while other reaction parameters were kept constant. For synthesis of MFHAs the optimum mol ratio of N-MHA/palm kernel oil = 6/1 and the highest conversion was 77.8%, for synthesis of IPFHAs the optimum mol ratio of N-IPHA/palm kernel oil = 7/1 and the highest conversion was 65.4% and for synthesis of BFHAs the optimum mol ratio of N-BHA/palm kernel oil = 7/1 and the highest conversion was 61.7%. MDPI 2011-08-05 /pmc/articles/PMC6264264/ /pubmed/25134767 http://dx.doi.org/10.3390/molecules16086634 Text en © 2011 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Jahangirian, Hossein Haron, Md Jelas Yusof, Nor Azah Silong, Sidik Kassim, Anuar Rafiee-Moghaddam, Roshanak Peyda, Mazyar Gharayebi, Yadollah Enzymatic Synthesis of Fatty Hydroxamic Acid Derivatives Based on Palm Kernel Oil |
title | Enzymatic Synthesis of Fatty Hydroxamic Acid Derivatives Based on Palm Kernel Oil |
title_full | Enzymatic Synthesis of Fatty Hydroxamic Acid Derivatives Based on Palm Kernel Oil |
title_fullStr | Enzymatic Synthesis of Fatty Hydroxamic Acid Derivatives Based on Palm Kernel Oil |
title_full_unstemmed | Enzymatic Synthesis of Fatty Hydroxamic Acid Derivatives Based on Palm Kernel Oil |
title_short | Enzymatic Synthesis of Fatty Hydroxamic Acid Derivatives Based on Palm Kernel Oil |
title_sort | enzymatic synthesis of fatty hydroxamic acid derivatives based on palm kernel oil |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6264264/ https://www.ncbi.nlm.nih.gov/pubmed/25134767 http://dx.doi.org/10.3390/molecules16086634 |
work_keys_str_mv | AT jahangirianhossein enzymaticsynthesisoffattyhydroxamicacidderivativesbasedonpalmkerneloil AT haronmdjelas enzymaticsynthesisoffattyhydroxamicacidderivativesbasedonpalmkerneloil AT yusofnorazah enzymaticsynthesisoffattyhydroxamicacidderivativesbasedonpalmkerneloil AT silongsidik enzymaticsynthesisoffattyhydroxamicacidderivativesbasedonpalmkerneloil AT kassimanuar enzymaticsynthesisoffattyhydroxamicacidderivativesbasedonpalmkerneloil AT rafieemoghaddamroshanak enzymaticsynthesisoffattyhydroxamicacidderivativesbasedonpalmkerneloil AT peydamazyar enzymaticsynthesisoffattyhydroxamicacidderivativesbasedonpalmkerneloil AT gharayebiyadollah enzymaticsynthesisoffattyhydroxamicacidderivativesbasedonpalmkerneloil |