611-41-6

Upstream product

• 156-43-4 4-Ethoxyaniline 
• 51992-13-3 N-(4-ethoxy-phenyl)-malamic acid 
• 100122-11-0 1-(4-ethoxy-phenyl)-3-chloro-pyrrolidine-2,5-dione 
• 19077-60-2 1-(4-ethoxyphenyl)-1H-pyrrole-2,5-dione 
• 110-15-6 succinic acid 
• 59256-45-0 N-(4-ethoxy-phenyl)-succinamic acid 
• 108-30-5 succinic acid anhydride 

Downstream Products

• 59256-45-0 N-(4-ethoxy-phenyl)-succinamic acid 

Relevant academic research and scientific papers

Solid-phase synthesis of N-aryl succinimides

A new method upon adopting a solid-phase strategy for synthesis of N-aryl succinimides is described here, using the silica-bound benzoyl chloride (SBBC) as dehydrating agent in reaction with N-arylsuccinamic acids. The main advantage of this method is the

α-chlorosuccinimides - A new source for maleimides and succinimides

N-Arylmaleimides and N-arylsuccinimides were prepared by dehydrochlorination reaction of N-aryl α-chlorosuccinimides in the presence of a base and by reduction of 2-chlorosuccinimide in the presence of zinc, respectively. N-Aryl α-chlorosuccinimides were obtained by dehydration of N-aryl substituted maleamic acids in the presence of thionyl chloride. The structure of the synthesized compounds was confirmed by IR, 1H-NMR and 13C-NMR spectra.