Please use this identifier to cite or link to this item: https://repository.sustech.edu/handle/123456789/13877
Title: Preparation of Some 4- diazo (hetero aryl)phenyl pyrazole and 2-diazo(hetero aryl) phenyl dimedone derivatives
Other Titles: تحضیر بعض مشتقات 4- دایا زو (ھیتیرواریل) فینیل بیرازولو 2 - دایزو(ھیتیرو اریل) فینیل دایمیدون
Authors: Abdu Alrahem, Raja Bashar Suleiman
Supervisor, Ahmed Elsadig Mohammed Saeed
Co. Supervisor, Amna BintWhab Elrashid Mohammed Hussein
Keywords: Chemistry
phenyl dimedone derivatives
hetero aryl
phenyl pyrazole and 2-diazo
Preparation of Some 4- diazo
Issue Date: 10-May-2016
Publisher: Sudan University of Science and Technology
Citation: Abdu Alrahem, Raja Bashar Suleiman . Preparation of Some 4- diazo (hetero aryl)phenyl pyrazole and 2-diazo(hetero aryl) phenyl dimedone derivatives / Raja Bashar Suleiman Abdu Alrahem ; Ahmed Elsadig Mohammed Saeed , Amna BintWhab Elrashid Mohammed Hussein .- Khartoum: Sudan University of Science and Technology, college of Science, 2016 .- 200p. :ill. ;28cm .-PhD.
Abstract: In the present work fifty six a new α, β - unsaturated carbonyl compounds and their cyclization reactions with varieties reagent (hydrazine derivatives, hydroxylamine and thio urea) pyrazole, isoxazole and thiopyrimidine derivatives were prepared. A process of the preparation of α, β – unsaturated carbonyl compounds by coupling to diazotized a p-aminoacetophenone with 1.3 di carbonyl compounds (ethyl acetoacetate, acetyl acetone, bezoylacetone and dimedone) in presence sodium acetate and ethanol (C-N) bond was formed. Some of the resultant compounds reacted with hydrazine derivatives lead to cyclized to the pyrazole derivatives and condensed with aromatic aldehyde give the synthesis α, β – unsaturated carbonyl. Later were prepared directly from some resultant of the coupling with dimedone in presence basic media sodium hydroxide at room temperature . The reaction progress for all synthesized compounds was checked by (TLC) technique , meting point, and yield percentage. The structure of synthesized compounds were confirmed by spectroscopic instruments IR, some of synthesized compound were confirmed by UV, IH-NMR, 13C-NMR, MS.
Description: Thesis
URI: http://repository.sustech.edu/handle/123456789/13877
Appears in Collections:PhD theses : Science

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