69338-50-7

Upstream product

• 85-44-9 phthalic anhydride 

Downstream Products

• 69338-58-5 N-s-Butyl-N'-t-butylphthalamid 
• 69338-60-9 N-cyclohexyl-N'-terbutylphthalamide 
• 69338-64-3 N-t-Butyl-N'-p-methoxyphenylphthalamid 
• 69338-67-6 N-t-Butyl-N'-p-nitrophenylphthalamid 
• 69338-59-6 benzene N,N'-di-tert-butyldicarboxamide 
• 69338-56-3 N-n-Butyl-N'-t-butylphthalamid 
• 69338-69-8 N-tert-Butyl-2-(N'-phenyl-hydrazinocarbonyl)-benzamide 
• 69338-61-0 N-Benzyl-N'-t-butyl-phthalimid 
• 80991-98-6 2-tert-Butylcarbamoyl-benzoyl azide 
• 56475-12-8 3-(tert-butylimino)isobenzofuran-1(3H)-one 
• 69338-63-2 N-t-Butyl-N'-m-methoxyphenylphthalamid 
• 69338-57-4 N-Isobutyl-N'-t-butylphthalamid 
• 69338-71-2 Ethyl-N-t-butylphthalamat 

Relevant academic research and scientific papers

Practical synthesis of phthalimides and benzamides by a multicomponent reaction involving arynes, isocyanides, and CO2/H2O

Transition-metal-free multicomponent reactions involving arynes and isocyanides with either CO2 or H2O have been reported. With CO2 as the third component, the reactions resulted in the formation of N-substituted phthalimides. The utility of water as the third component furnished benzamide derivatives in moderate to good yields. These reactions took place under mild conditions with broad scope.