Syntheses of 2,3-dioxopyrrolidines with anisaldehyde using different amines / Norhabibah Mohamad

2,3-dioxopyrrolidines were synthesized using anisaldehyde with different amines in a suspension of sodium diethyl oxalacetate (1 equiv), amine (1 equiv) and anisaldehyde (1 equiv) in ethanol. Three different amines were used and they were methylamine, benzylamine and isopropylamine. Many possibilit...

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Main Author: Mohamad, Norhabibah
Format: Thesis
Language:English
Published: 2009
Online Access:https://ir.uitm.edu.my/id/eprint/103323/1/103323.pdf
https://ir.uitm.edu.my/id/eprint/103323/
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Institution: Universiti Teknologi Mara
Language: English
id my.uitm.ir.103323
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spelling my.uitm.ir.1033232024-09-28T16:03:32Z https://ir.uitm.edu.my/id/eprint/103323/ Syntheses of 2,3-dioxopyrrolidines with anisaldehyde using different amines / Norhabibah Mohamad Mohamad, Norhabibah 2,3-dioxopyrrolidines were synthesized using anisaldehyde with different amines in a suspension of sodium diethyl oxalacetate (1 equiv), amine (1 equiv) and anisaldehyde (1 equiv) in ethanol. Three different amines were used and they were methylamine, benzylamine and isopropylamine. Many possibilities of syntheses products of 2,3- Dioxopyrrolidines were investigated. 2,3-Dioxopyrrolidines obtained were in moderate yields but of high purity. A significant advantage of these products was that most of them can be crystallized out of the reaction mixture. The synthesized compounds can lead towards the syntheses of biologically active natural products. The compounds were also reduced using zinc powder in the presence of acid. Reduction of synthesized 2,3- Dioxopyrrolidines gave the corresponding secondary alcohols. 2009 Thesis NonPeerReviewed text en https://ir.uitm.edu.my/id/eprint/103323/1/103323.pdf Syntheses of 2,3-dioxopyrrolidines with anisaldehyde using different amines / Norhabibah Mohamad. (2009) Degree thesis, thesis, Universiti Teknologi MARA (UiTM). <http://terminalib.uitm.edu.my/103323.pdf>
institution Universiti Teknologi Mara
building Tun Abdul Razak Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Teknologi Mara
content_source UiTM Institutional Repository
url_provider http://ir.uitm.edu.my/
language English
description 2,3-dioxopyrrolidines were synthesized using anisaldehyde with different amines in a suspension of sodium diethyl oxalacetate (1 equiv), amine (1 equiv) and anisaldehyde (1 equiv) in ethanol. Three different amines were used and they were methylamine, benzylamine and isopropylamine. Many possibilities of syntheses products of 2,3- Dioxopyrrolidines were investigated. 2,3-Dioxopyrrolidines obtained were in moderate yields but of high purity. A significant advantage of these products was that most of them can be crystallized out of the reaction mixture. The synthesized compounds can lead towards the syntheses of biologically active natural products. The compounds were also reduced using zinc powder in the presence of acid. Reduction of synthesized 2,3- Dioxopyrrolidines gave the corresponding secondary alcohols.
format Thesis
author Mohamad, Norhabibah
spellingShingle Mohamad, Norhabibah
Syntheses of 2,3-dioxopyrrolidines with anisaldehyde using different amines / Norhabibah Mohamad
author_facet Mohamad, Norhabibah
author_sort Mohamad, Norhabibah
title Syntheses of 2,3-dioxopyrrolidines with anisaldehyde using different amines / Norhabibah Mohamad
title_short Syntheses of 2,3-dioxopyrrolidines with anisaldehyde using different amines / Norhabibah Mohamad
title_full Syntheses of 2,3-dioxopyrrolidines with anisaldehyde using different amines / Norhabibah Mohamad
title_fullStr Syntheses of 2,3-dioxopyrrolidines with anisaldehyde using different amines / Norhabibah Mohamad
title_full_unstemmed Syntheses of 2,3-dioxopyrrolidines with anisaldehyde using different amines / Norhabibah Mohamad
title_sort syntheses of 2,3-dioxopyrrolidines with anisaldehyde using different amines / norhabibah mohamad
publishDate 2009
url https://ir.uitm.edu.my/id/eprint/103323/1/103323.pdf
https://ir.uitm.edu.my/id/eprint/103323/
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