Preparation of Fatty Amides from Metal Soaps Under Microwave Irradiation

An efficient, high yield method of preparation of pure fatty amides was found through this research. from the 3 - reactant system that consists of fatty sodium soap, a source o f ammonia (or amine) and ammonium chloride, the fatty amides were formed when they were premixed and sealed in a glass v...

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Main Author: Lee, Yean Kee
Format: Thesis
Language:English
English
Published: 2002
Online Access:http://psasir.upm.edu.my/id/eprint/9529/1/FSAS_2002_60_A.pdf
http://psasir.upm.edu.my/id/eprint/9529/
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spelling my.upm.eprints.95292012-05-18T04:05:18Z http://psasir.upm.edu.my/id/eprint/9529/ Preparation of Fatty Amides from Metal Soaps Under Microwave Irradiation Lee, Yean Kee An efficient, high yield method of preparation of pure fatty amides was found through this research. from the 3 - reactant system that consists of fatty sodium soap, a source o f ammonia (or amine) and ammonium chloride, the fatty amides were formed when they were premixed and sealed in a glass vessel and then exposed to microwave irradiation. Primary amides were formed from the reaction of fatty sodium soap, urea or ammonium carbonate and ammonium chloride, whereas secondary amides were formed from the reaction of fatty sodium soap, amines and ammonium chloride. Primary amides successfully synthesized through this method are myristamide, palmitamide, o leamide and stearamide, whereas secondary amides synthesized from this method are N-butyl myristamide, N-butyl palmitamide, N-butyl stearamide, Nhexadecyl myristamide, N-hexadecyl palmitamide, and N-hexadecyl stearamide. Product identification was done through lR, NMR and CHN . The syntheses of myristamide and palmitamide were optimized by varying the irradiation time, reactant ratio and volume of reaction vessels. These optimized conditions were used for other primary amides syntheses. It was found that the best reactant ratio (sodium soap : urea: ammonium chloride) is 1:0.5:1 with 2.5 cm³ volume of reaction vessel when 0.5 g of reactant mixture were irradiated for 9 minutes. In the two or three-reactant systems involving fatty acids and, or sodium soap with urea or ammonium carbonate as the source of ammon ia, the presence or absence of ammonium chloride in these reactant mixtures were studied. The reaction involving soaps required the three-reactant system, where ammonium chloride is present in the reactant mixture. A kinetic study of the synthesis of palmitamide was done. The decomposition of sodium palmitate was found to fit first order kinetics and hence a reaction mechanism was proposed. Palm oil soap was also used in the amide syntheses and mixtures of primary amides were successfully synthesized from the reaction between palm oil soap, urea and ammonium chloride. 2002-12 Thesis NonPeerReviewed application/pdf en http://psasir.upm.edu.my/id/eprint/9529/1/FSAS_2002_60_A.pdf Lee, Yean Kee (2002) Preparation of Fatty Amides from Metal Soaps Under Microwave Irradiation. Masters thesis, Universiti Putra Malaysia. English
institution Universiti Putra Malaysia
building UPM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Putra Malaysia
content_source UPM Institutional Repository
url_provider http://psasir.upm.edu.my/
language English
English
description An efficient, high yield method of preparation of pure fatty amides was found through this research. from the 3 - reactant system that consists of fatty sodium soap, a source o f ammonia (or amine) and ammonium chloride, the fatty amides were formed when they were premixed and sealed in a glass vessel and then exposed to microwave irradiation. Primary amides were formed from the reaction of fatty sodium soap, urea or ammonium carbonate and ammonium chloride, whereas secondary amides were formed from the reaction of fatty sodium soap, amines and ammonium chloride. Primary amides successfully synthesized through this method are myristamide, palmitamide, o leamide and stearamide, whereas secondary amides synthesized from this method are N-butyl myristamide, N-butyl palmitamide, N-butyl stearamide, Nhexadecyl myristamide, N-hexadecyl palmitamide, and N-hexadecyl stearamide. Product identification was done through lR, NMR and CHN . The syntheses of myristamide and palmitamide were optimized by varying the irradiation time, reactant ratio and volume of reaction vessels. These optimized conditions were used for other primary amides syntheses. It was found that the best reactant ratio (sodium soap : urea: ammonium chloride) is 1:0.5:1 with 2.5 cm³ volume of reaction vessel when 0.5 g of reactant mixture were irradiated for 9 minutes. In the two or three-reactant systems involving fatty acids and, or sodium soap with urea or ammonium carbonate as the source of ammon ia, the presence or absence of ammonium chloride in these reactant mixtures were studied. The reaction involving soaps required the three-reactant system, where ammonium chloride is present in the reactant mixture. A kinetic study of the synthesis of palmitamide was done. The decomposition of sodium palmitate was found to fit first order kinetics and hence a reaction mechanism was proposed. Palm oil soap was also used in the amide syntheses and mixtures of primary amides were successfully synthesized from the reaction between palm oil soap, urea and ammonium chloride.
format Thesis
author Lee, Yean Kee
spellingShingle Lee, Yean Kee
Preparation of Fatty Amides from Metal Soaps Under Microwave Irradiation
author_facet Lee, Yean Kee
author_sort Lee, Yean Kee
title Preparation of Fatty Amides from Metal Soaps Under Microwave Irradiation
title_short Preparation of Fatty Amides from Metal Soaps Under Microwave Irradiation
title_full Preparation of Fatty Amides from Metal Soaps Under Microwave Irradiation
title_fullStr Preparation of Fatty Amides from Metal Soaps Under Microwave Irradiation
title_full_unstemmed Preparation of Fatty Amides from Metal Soaps Under Microwave Irradiation
title_sort preparation of fatty amides from metal soaps under microwave irradiation
publishDate 2002
url http://psasir.upm.edu.my/id/eprint/9529/1/FSAS_2002_60_A.pdf
http://psasir.upm.edu.my/id/eprint/9529/
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score 13.160551