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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Main Author: Uzairi, Nor Aisah
Format: Thesis
Language:English
Published: 2008
Online Access:https://ir.uitm.edu.my/id/eprint/102106/1/102106.pdf
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spelling 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
institution Universiti Teknologi MARA
collection UiTM Institutional Repository
language English
advisor -, 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
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