Coumarins - fast synthesis by the knoevenagel condensation under microwave irradiation / Rahmat Mohamed Tahir

Coumarin nowadays is of great importance especially in the area of pharmaceutical. Therefore, a faster way of producing coumarin was needed while maintaining the purity and yields of product as high as possible. One of the methods is Knoevenagel condensation under microwave assisted irradiation. Thi...

Full description

Saved in:
Bibliographic Details
Main Author: Mohamed Tahir, Rahmat
Format: Thesis
Language:en
Published: 2008
Subjects:
Online Access:https://ir.uitm.edu.my/id/eprint/101908/1/101908.PDF
https://ir.uitm.edu.my/id/eprint/101908/
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1833322142260789248
author Mohamed Tahir, Rahmat
author_facet Mohamed Tahir, Rahmat
author_sort Mohamed Tahir, Rahmat
building Tun Abdul Razak Library
collection Institutional Repository
content_provider Universiti Teknologi Mara
content_source UiTM Institutional Repository
continent Asia
country Malaysia
description Coumarin nowadays is of great importance especially in the area of pharmaceutical. Therefore, a faster way of producing coumarin was needed while maintaining the purity and yields of product as high as possible. One of the methods is Knoevenagel condensation under microwave assisted irradiation. This research was aimed to prove that under the microwave irradiation the Knoevenagel condensation can be successfully applied to the synthesis of a number of coumarins. Also, the researcher wanted to find the most suitable base for this reaction. 2-hydroxy-4-methoxy benzaldehyde and 2- hydroxy-5-methoxy benzaldehyde were reacted with diethyl melonate in the presence of three different bases; diethylamine, pyridine, and potassium tert-butoxide for three different reactions. The reactions were set under different conditions: stirring with no heating for six hours; stirring with heating at 80°C for six hours; and under microwave assisted irradiation at 1000 watt power, 70°C, and stirring speed of I 00 rpm for one hour. TLC was used to prove the reactions were completed. To confirm the structure of coumarins (13 and 16) formed, 1H and 13C-NMR analyses were used. From the results, it was found out that diethylamine was the most suitable base for this reaction therefore used throughout the research. Productions of coumarins were significantly increased from stirring, no heating condition (29.07 % and 61.13 %) to stirring, heating condition (39.52 % and 68.23 %) to microwave assisted irradiation (48.39 % and 84.68 %). The time for reaction under microwave condition was also decreased to one hour and yet the percentage yield was still maintained.
format Thesis
id my.uitm.ir-101908
institution Universiti Teknologi Mara
language en
publishDate 2008
record_format eprints
spelling my.uitm.ir-1019082024-09-28T23:34:49Z https://ir.uitm.edu.my/id/eprint/101908/ Coumarins - fast synthesis by the knoevenagel condensation under microwave irradiation / Rahmat Mohamed Tahir Mohamed Tahir, Rahmat Pharmacopoeias Materia medica Coumarin nowadays is of great importance especially in the area of pharmaceutical. Therefore, a faster way of producing coumarin was needed while maintaining the purity and yields of product as high as possible. One of the methods is Knoevenagel condensation under microwave assisted irradiation. This research was aimed to prove that under the microwave irradiation the Knoevenagel condensation can be successfully applied to the synthesis of a number of coumarins. Also, the researcher wanted to find the most suitable base for this reaction. 2-hydroxy-4-methoxy benzaldehyde and 2- hydroxy-5-methoxy benzaldehyde were reacted with diethyl melonate in the presence of three different bases; diethylamine, pyridine, and potassium tert-butoxide for three different reactions. The reactions were set under different conditions: stirring with no heating for six hours; stirring with heating at 80°C for six hours; and under microwave assisted irradiation at 1000 watt power, 70°C, and stirring speed of I 00 rpm for one hour. TLC was used to prove the reactions were completed. To confirm the structure of coumarins (13 and 16) formed, 1H and 13C-NMR analyses were used. From the results, it was found out that diethylamine was the most suitable base for this reaction therefore used throughout the research. Productions of coumarins were significantly increased from stirring, no heating condition (29.07 % and 61.13 %) to stirring, heating condition (39.52 % and 68.23 %) to microwave assisted irradiation (48.39 % and 84.68 %). The time for reaction under microwave condition was also decreased to one hour and yet the percentage yield was still maintained. 2008 Thesis NonPeerReviewed text en https://ir.uitm.edu.my/id/eprint/101908/1/101908.PDF Coumarins - fast synthesis by the knoevenagel condensation under microwave irradiation / Rahmat Mohamed Tahir. (2008) Degree thesis, thesis, Universiti Teknologi MARA (Kampus Puncak Alam).
spellingShingle Pharmacopoeias
Materia medica
Mohamed Tahir, Rahmat
Coumarins - fast synthesis by the knoevenagel condensation under microwave irradiation / Rahmat Mohamed Tahir
title Coumarins - fast synthesis by the knoevenagel condensation under microwave irradiation / Rahmat Mohamed Tahir
title_full Coumarins - fast synthesis by the knoevenagel condensation under microwave irradiation / Rahmat Mohamed Tahir
title_fullStr Coumarins - fast synthesis by the knoevenagel condensation under microwave irradiation / Rahmat Mohamed Tahir
title_full_unstemmed Coumarins - fast synthesis by the knoevenagel condensation under microwave irradiation / Rahmat Mohamed Tahir
title_short Coumarins - fast synthesis by the knoevenagel condensation under microwave irradiation / Rahmat Mohamed Tahir
title_sort coumarins - fast synthesis by the knoevenagel condensation under microwave irradiation / rahmat mohamed tahir
topic Pharmacopoeias
Materia medica
url https://ir.uitm.edu.my/id/eprint/101908/1/101908.PDF
https://ir.uitm.edu.my/id/eprint/101908/
url_provider http://ir.uitm.edu.my/