Psynthesis of a substituted cyclohexenone via Michael addition and intramolecular aldol condensation (Robinson annulation) of chalcone with ethyl acetoacetate / Nor Aisah Uzairi
Ethyl 6-(4-methoxyphenyl)-4-phenylcyclohex-3-en-2-one-l-carboxylate was synthesized through Michael addition and intramolecular aldol condensation (Robinson annulation) of 4-methoxychalcone with ethyl acetoacetate using a strong base, natrium hydroxyde (NaOH) as catalyst. 4-mthoxychalcone was first...
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2008
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my-uitm-ir.1021062024-09-12T16:29:05Z Psynthesis of a substituted cyclohexenone via Michael addition and intramolecular aldol condensation (Robinson annulation) of chalcone with ethyl acetoacetate / Nor Aisah Uzairi 2008 Uzairi, Nor Aisah Ethyl 6-(4-methoxyphenyl)-4-phenylcyclohex-3-en-2-one-l-carboxylate was synthesized through Michael addition and intramolecular aldol condensation (Robinson annulation) of 4-methoxychalcone with ethyl acetoacetate using a strong base, natrium hydroxyde (NaOH) as catalyst. 4-mthoxychalcone was first prepared by aldol condensation of 4-methoxybenzaldehyde and acetophenone. The percentage yield of 4- methoxychalcone was 98.65% and its melting point is 74-75°C. Then 4-Methoxychalcone was reacted with ethyl acetoacetate through Michael addition and aldol cyclization to form the final substituted cyclohexenone product in 79% yield. The melting point of the substituted cyclohexenone product is 108 - 110°C. 2008 Thesis https://ir.uitm.edu.my/id/eprint/102106/ https://ir.uitm.edu.my/id/eprint/102106/1/102106.pdf text en public degree Universiti Teknologi MARA (UiTM) Faculty of Applied Sciences -, Yazan |
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Universiti Teknologi MARA |
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UiTM Institutional Repository |
language |
English |
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-, Yazan |
description |
Ethyl 6-(4-methoxyphenyl)-4-phenylcyclohex-3-en-2-one-l-carboxylate was synthesized through Michael addition and intramolecular aldol condensation (Robinson annulation) of 4-methoxychalcone with ethyl acetoacetate using a strong base, natrium hydroxyde (NaOH) as catalyst. 4-mthoxychalcone was first prepared by aldol condensation of 4-methoxybenzaldehyde and acetophenone. The percentage yield of 4- methoxychalcone was 98.65% and its melting point is 74-75°C. Then 4-Methoxychalcone was reacted with ethyl acetoacetate through Michael addition and aldol cyclization to form the final substituted cyclohexenone product in 79% yield. The melting point of the substituted cyclohexenone product is 108 - 110°C. |
format |
Thesis |
qualification_level |
Bachelor degree |
author |
Uzairi, Nor Aisah |
spellingShingle |
Uzairi, Nor Aisah Psynthesis of a substituted cyclohexenone via Michael addition and intramolecular aldol condensation (Robinson annulation) of chalcone with ethyl acetoacetate / Nor Aisah Uzairi |
author_facet |
Uzairi, Nor Aisah |
author_sort |
Uzairi, Nor Aisah |
title |
Psynthesis of a substituted cyclohexenone via Michael addition and intramolecular aldol condensation (Robinson annulation) of chalcone with ethyl acetoacetate / Nor Aisah Uzairi |
title_short |
Psynthesis of a substituted cyclohexenone via Michael addition and intramolecular aldol condensation (Robinson annulation) of chalcone with ethyl acetoacetate / Nor Aisah Uzairi |
title_full |
Psynthesis of a substituted cyclohexenone via Michael addition and intramolecular aldol condensation (Robinson annulation) of chalcone with ethyl acetoacetate / Nor Aisah Uzairi |
title_fullStr |
Psynthesis of a substituted cyclohexenone via Michael addition and intramolecular aldol condensation (Robinson annulation) of chalcone with ethyl acetoacetate / Nor Aisah Uzairi |
title_full_unstemmed |
Psynthesis of a substituted cyclohexenone via Michael addition and intramolecular aldol condensation (Robinson annulation) of chalcone with ethyl acetoacetate / Nor Aisah Uzairi |
title_sort |
psynthesis of a substituted cyclohexenone via michael addition and intramolecular aldol condensation (robinson annulation) of chalcone with ethyl acetoacetate / nor aisah uzairi |
granting_institution |
Universiti Teknologi MARA (UiTM) |
granting_department |
Faculty of Applied Sciences |
publishDate |
2008 |
url |
https://ir.uitm.edu.my/id/eprint/102106/1/102106.pdf |
_version_ |
1811769208810242048 |