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  • Synthesis of new azo compounds based on N-(4-hydroxypheneyl)maleimide and N-(4-methylpheneyl)maleimide.

Synthesis of new azo compounds based on N-(4-hydroxypheneyl)maleimide and N-(4-methylpheneyl)maleimide.

Molecules (Basel, Switzerland) (2010-10-27)
Issam Ahmed Mohammed, Asniza Mustapha
ABSTRACT

Maleic anhydride was reacted with p-aminophenol and p-toluidine in the presence of di-phosphorus pentoxide (P₂O₅) as a catalyst to produce two compounds: N-(4-hydroxy-phenyl)maleimide (I) and N-(4-methylphenyl)maleimide (II). The new azo compounds I(a-c) and II(a-c) were prepared by the reaction of I and II with three different aromatic amines, namely aniline, p-aminophenol and p-toluidine. The structures of these compounds were confirmed by CHN, FT-IR, ¹H-NMR, ¹³C-NMR, mass spectrum and UV/Vis spectroscopy.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
p-Toluidine hydrochloride, purum, ≥99.0% (AT)
Supelco
p-Toluidine, for spectrophotometric det. of Au, Tl(III), W, ≥99.0%
Sigma-Aldrich
p-Toluidine, 99%
Sigma-Aldrich
p-Toluidine, 99.6%