73823-19-5

Upstream product

• 18815-75-3 N-(4-bromobenzyl-1-carbonyl)-glycine 
• 586-76-5 4-Bromobenzoic acid 
• 27466-83-7 4-bromo-N-methylbenzamide 
• 698-67-9 p-bromobenzamide 
• 586-75-4 4-chlorobenzoyl chloride 
• 73823-15-1 4-bromo-N-((dimethylamino)methylene)benzamide 

Relevant academic research and scientific papers

Visible-Light-Driven Oxidation of N -Alkylamides to Imides Using Oxone/H 2 O and Catalytic KBr

Imides are prepared conveniently by visible-light-driven oxidations of various N -alkylamides under mild conditions. The majority of the reactions proceed efficiently by using Oxone as the oxidant in the presence of a catalytic amount of KBr in H 2 O/CH 2 Cl 2 under irradiation by an 8 W white LED at room temperature. Experimental studies suggest that an imine, obtained from the substrate amide via a radical process, is the key intermediate.

An efficient method for the preparation of N-formyl-imide via amidine using propylphosphonic anhydride (T3P)

An efficient method for the preparation of N-formyl imide via amidine using propylphosphonic anhydride (T3P) has been described. Using this method many aryl, hetero aryl, alkyl as well as amino acid imides were synthesized in high yields.

A facile synthesis of N-formylbenzamides by oxidative decarboxylation of N-aroylglycine induced by Ag+/S2O82-

A facile method is described for the synthesis of N-formylbenzamides by oxidative decarboxylation of N-aroylglycine using catalytic silver(I) and 2 equivalents of ammonium persulfate as an oxidant in a biphasic system (CHCl 3/water).