Cyclohexyldiphenylphosphine in heck coupling / Nurulhidayah Abdul Kader

This study describes mainly the significance of phosphine ligand that is cyclohexyldiphenylphosphine. Phosphine ligand have been used in Heck reaction together with other conditions chosen such as silver nitrate, potassium acetate, palladium chloride and dimethylformamide to synthesise stilbene that...

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Main Author: Abdul Kader, Nurulhidayah
Format: Thesis
Language:en
Published: 2008
Subjects:
Online Access:https://ir.uitm.edu.my/id/eprint/101199/1/101199.PDF
https://ir.uitm.edu.my/id/eprint/101199/
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author Abdul Kader, Nurulhidayah
author_facet Abdul Kader, Nurulhidayah
author_sort Abdul Kader, Nurulhidayah
building Tun Abdul Razak Library
collection Institutional Repository
content_provider Universiti Teknologi Mara
content_source UiTM Institutional Repository
continent Asia
country Malaysia
description This study describes mainly the significance of phosphine ligand that is cyclohexyldiphenylphosphine. Phosphine ligand have been used in Heck reaction together with other conditions chosen such as silver nitrate, potassium acetate, palladium chloride and dimethylformamide to synthesise stilbene that is 3,4-dimethoxy- 12-acetoxystilbene. All reaction conditions chosen were appropriate to synthesise the desired compound. This study was carried out using Heck reaction to achieve the objective of this study. Heck reaction was found to be the efficient method. Prior to Heck reaction, the hydroxyl group in 4-iodophenol was protected by forming 4- iodophenylacetate. The coupling of 4-iodophenylacetate with 3,4-dimethoxystyrene gave 3,4-dimethoxy-12-acetoxystilbene. The product was analyzed using TLC and extracted using ethyl acetate and hexane. Purification of the reaction product was done by using column chromatography. The chemical structure of stilbene was confirmed by nuclear magnetic resonance spectroscopy.
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publishDate 2008
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spelling my.uitm.ir-1011992024-09-28T23:17:21Z https://ir.uitm.edu.my/id/eprint/101199/ Cyclohexyldiphenylphosphine in heck coupling / Nurulhidayah Abdul Kader Abdul Kader, Nurulhidayah Pharmaceutical chemistry This study describes mainly the significance of phosphine ligand that is cyclohexyldiphenylphosphine. Phosphine ligand have been used in Heck reaction together with other conditions chosen such as silver nitrate, potassium acetate, palladium chloride and dimethylformamide to synthesise stilbene that is 3,4-dimethoxy- 12-acetoxystilbene. All reaction conditions chosen were appropriate to synthesise the desired compound. This study was carried out using Heck reaction to achieve the objective of this study. Heck reaction was found to be the efficient method. Prior to Heck reaction, the hydroxyl group in 4-iodophenol was protected by forming 4- iodophenylacetate. The coupling of 4-iodophenylacetate with 3,4-dimethoxystyrene gave 3,4-dimethoxy-12-acetoxystilbene. The product was analyzed using TLC and extracted using ethyl acetate and hexane. Purification of the reaction product was done by using column chromatography. The chemical structure of stilbene was confirmed by nuclear magnetic resonance spectroscopy. 2008 Thesis NonPeerReviewed text en https://ir.uitm.edu.my/id/eprint/101199/1/101199.PDF Cyclohexyldiphenylphosphine in heck coupling / Nurulhidayah Abdul Kader. (2008) Degree thesis, thesis, Universiti Teknologi MARA (Kampus Puncak Alam).
spellingShingle Pharmaceutical chemistry
Abdul Kader, Nurulhidayah
Cyclohexyldiphenylphosphine in heck coupling / Nurulhidayah Abdul Kader
title Cyclohexyldiphenylphosphine in heck coupling / Nurulhidayah Abdul Kader
title_full Cyclohexyldiphenylphosphine in heck coupling / Nurulhidayah Abdul Kader
title_fullStr Cyclohexyldiphenylphosphine in heck coupling / Nurulhidayah Abdul Kader
title_full_unstemmed Cyclohexyldiphenylphosphine in heck coupling / Nurulhidayah Abdul Kader
title_short Cyclohexyldiphenylphosphine in heck coupling / Nurulhidayah Abdul Kader
title_sort cyclohexyldiphenylphosphine in heck coupling / nurulhidayah abdul kader
topic Pharmaceutical chemistry
url https://ir.uitm.edu.my/id/eprint/101199/1/101199.PDF
https://ir.uitm.edu.my/id/eprint/101199/
url_provider http://ir.uitm.edu.my/