Synthesis of 4-acetoxy-ll,13- dibenzyloxystilbene / Nor Hayati Abu Samah

The main objective of this project is to synthesize a stilbene analogue, 4-acetoxy-l 1,13- dibenzyloxystilbene at large scale in order to supply for bioactivity and reactivity investigations by other researchers. Three established reactions have been used in order to accomplish the project. First, t...

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Main Author: Abu Samah, Nor Hayati
Format: Thesis
Language:English
Published: 2005
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Online Access:https://ir.uitm.edu.my/id/eprint/98657/1/98657.PDF
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spelling my-uitm-ir.986572024-07-22T08:02:14Z Synthesis of 4-acetoxy-ll,13- dibenzyloxystilbene / Nor Hayati Abu Samah 2005 Abu Samah, Nor Hayati RM Therapeutics. Pharmacology RS Pharmacy and materia medica The main objective of this project is to synthesize a stilbene analogue, 4-acetoxy-l 1,13- dibenzyloxystilbene at large scale in order to supply for bioactivity and reactivity investigations by other researchers. Three established reactions have been used in order to accomplish the project. First, the protection ofp-iodophenol using acetic anhydride to yield p-iodophenylacetale followed by the protection of 3,5-dihydroxybenzaldehyde with benzyl bromide that produced 3,5-dibenzyloxybenzaldehyde. Subsequently, the 3,5-dibenzyloxybenzaldehyde is utilized as a starting material of the Wittig reaction. Product of the Wittig reaction and /j-iodophenylaceate are then used to synthesize the stilbene analogue. The synthesized compounds are then, purified by chromatographic techniques and sent for 'H-NMR characterization. Concisely, even though the compound of desired has failed to be obtained, an almost structurally identical compound has been successfully synthesized in small amount. 2005 Thesis https://ir.uitm.edu.my/id/eprint/98657/ https://ir.uitm.edu.my/id/eprint/98657/1/98657.PDF text en public degree Universiti Teknologi MARA (Kampus Puncak Alam) Faculty of Pharmacy Abdul Wahab, Ibtisam
institution Universiti Teknologi MARA
collection UiTM Institutional Repository
language English
advisor Abdul Wahab, Ibtisam
topic RM Therapeutics
Pharmacology
RS Pharmacy and materia medica
spellingShingle RM Therapeutics
Pharmacology
RS Pharmacy and materia medica
Abu Samah, Nor Hayati
Synthesis of 4-acetoxy-ll,13- dibenzyloxystilbene / Nor Hayati Abu Samah
description The main objective of this project is to synthesize a stilbene analogue, 4-acetoxy-l 1,13- dibenzyloxystilbene at large scale in order to supply for bioactivity and reactivity investigations by other researchers. Three established reactions have been used in order to accomplish the project. First, the protection ofp-iodophenol using acetic anhydride to yield p-iodophenylacetale followed by the protection of 3,5-dihydroxybenzaldehyde with benzyl bromide that produced 3,5-dibenzyloxybenzaldehyde. Subsequently, the 3,5-dibenzyloxybenzaldehyde is utilized as a starting material of the Wittig reaction. Product of the Wittig reaction and /j-iodophenylaceate are then used to synthesize the stilbene analogue. The synthesized compounds are then, purified by chromatographic techniques and sent for 'H-NMR characterization. Concisely, even though the compound of desired has failed to be obtained, an almost structurally identical compound has been successfully synthesized in small amount.
format Thesis
qualification_level Bachelor degree
author Abu Samah, Nor Hayati
author_facet Abu Samah, Nor Hayati
author_sort Abu Samah, Nor Hayati
title Synthesis of 4-acetoxy-ll,13- dibenzyloxystilbene / Nor Hayati Abu Samah
title_short Synthesis of 4-acetoxy-ll,13- dibenzyloxystilbene / Nor Hayati Abu Samah
title_full Synthesis of 4-acetoxy-ll,13- dibenzyloxystilbene / Nor Hayati Abu Samah
title_fullStr Synthesis of 4-acetoxy-ll,13- dibenzyloxystilbene / Nor Hayati Abu Samah
title_full_unstemmed Synthesis of 4-acetoxy-ll,13- dibenzyloxystilbene / Nor Hayati Abu Samah
title_sort synthesis of 4-acetoxy-ll,13- dibenzyloxystilbene / nor hayati abu samah
granting_institution Universiti Teknologi MARA (Kampus Puncak Alam)
granting_department Faculty of Pharmacy
publishDate 2005
url https://ir.uitm.edu.my/id/eprint/98657/1/98657.PDF
_version_ 1811768951675289600