72374-63-1

Upstream product

• 106-49-0 p-toluidine 
• 93-55-0 1-phenyl-propan-1-one 

Downstream Products

• 86605-71-2 3-Methyl-2,6-diphenyl-1-p-tolyl-1H-pyridin-4-one 
• 10266-13-4 2,4-Diphenyl-3-methylquinoline 
• 109704-24-7 3,6-dimethyl-2,4-diphenylquinoline 
• 15753-61-4 1-phenyl-3-(p-tolylamino)prop-2-en-1-one 
• 77821-65-9 3-(2-Hydroxy-ethyl)-4-methyl-5-phenyl-1-p-tolyl-1,5-dihydro-pyrrol-2-one 
• 72374-72-2 N-1-(2,2-Dichlor-1-phenyl-propyliden)-p-methyl-anilin 
• 77821-57-9 (4-Methyl-2-oxo-5-phenyl-1-p-tolyl-2,5-dihydro-1H-pyrrol-3-yl)-acetic acid ethyl ester 
• 71115-30-5 2-Methyl-3-(4-methylphenylamino)-1,3-diphenyl-2-propenimine 

Relevant academic research and scientific papers

Oxidative rearrangement of ketimines to amides by MCPBA and BF3·OEt2

Several amides were obtained by an efficient method from the corresponding alkyl aryl ketimines in high yields. Ketimines are readily prepared from the corresponding ketones. This procedure involves the oxidation of alkyl aryl ketimines with MCPBA with BF3·OEt2. In this reaction, only aryl group of alkyl aryl ketimines was migrated to the electron deficient nitrogen atom.