Title of article
Formation of 1,5-Disubstituted 2-hydroxypyrroles via Reaction of 2-(Triphenylphosphoranylidene) succinic Anhydride with Schiff s Bases
Author/Authors
abid, obaid h. university of fallujah, Iraq , mahdy, omar g. university of anbar - college of education for pure science, Iraq
From page
34
To page
40
Abstract
Schiff s Bases were synthesized from the reaction of furfuraldehyde and substituted benzaldehyde with 4-aminoantipyrine and 2,4-dinitrophenylhydrazine and reacted with 2-(triphenylphosphoranylidene) succinic anhydride in an anhydrous 1,4- dioxane at reflux conditions. The resulting products were found to be 1,5-disubstituted 2-hydroxypyrroles. The structures of the products were confirmed by their melting points, FT-IR, 1HNMR spectra and C.H.N. elemental analyses .
Keywords
Schiff s Bases , 1 , 5 , Disubstituted 2 , hydroxypyrroles
Journal title
Journal Of University Of Anbar For Pure Science
Journal title
Journal Of University Of Anbar For Pure Science
Record number
2598418
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