Abstract
Chloroacetamide derivatives (2a-g) have been prepared through reaction of chloroacetyl chloride(1) (which prepared by the reaction of chloroacetic acid with thionyl chloride) with primary aromatic amines and sulfa compounds to afford compounds (2a-g) which then reacted with p-hydroxy benzaldehyde via Williamson reaction to obtaine the new compounds 2-(4-formyl phenoxy)-N-aryl acetamide (3a-g). Finally , compounds (3a-g) will be use as a good synthon to prepare the Schiff bases represented by compounds 2-(4-aryliminophenoxy)-N-arylacetamide (4a-g). through , reaction with some primary aromatic amine. All the prepared compounds were investigated by the available physical and spectroscopic methods.
Keywords
Schiff base, amides, ether.
Article Type
Article
How to Cite this Article
Mauf, Ruwa M.; Sultan, Asmaa H.; and Farag, Ameera M
(2014)
"Synthesis of Some new 2-(4-Aryliminophenoxy)N-Arylacetamide Via p-hydroxy benzaldehyde.,"
Baghdad Science Journal: Vol. 11:
Iss.
2, Article 35.
DOI: https://doi.org/10.21123/bsj.2014.11.2.486-490
