Synthesis of Some new 2-(4-Aryliminophenoxy)N-Arylacetamide Via p-hydroxy benzaldehyde.

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Ruwa M. Mauf
Asmaa H. Sultan
AmeeraM Farag

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.

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1.
Synthesis of Some new 2-(4-Aryliminophenoxy)N-Arylacetamide Via p-hydroxy benzaldehyde. Baghdad Sci.J [Internet]. 2014 Jun. 1 [cited 2024 Mar. 29];11(2):486-90. Available from: https://bsj.uobaghdad.edu.iq/index.php/BSJ/article/view/2654
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How to Cite

1.
Synthesis of Some new 2-(4-Aryliminophenoxy)N-Arylacetamide Via p-hydroxy benzaldehyde. Baghdad Sci.J [Internet]. 2014 Jun. 1 [cited 2024 Mar. 29];11(2):486-90. Available from: https://bsj.uobaghdad.edu.iq/index.php/BSJ/article/view/2654

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