117332-22-6

Upstream product

• 1613-92-9 (E)-N-benzylidene-4-toluidine 
• 38879-46-8 (Z)-4-benzylidene-2-methyl-5(4H)-oxazolone 
• 2272-45-9 benzal-p-toluidine 
• 115127-03-2 N-cinnamoylamino glycine 
• 100-52-7 benzaldehyde 
• 94208-82-9 2-Methyl-5-[1-phenyl-meth-(Z)-ylidene]-3-p-tolyl-3,5-dihydro-imidazol-4-one 
• 117332-17-9 (Z)-2-Acetylamino-3-phenyl-N-p-tolyl-acrylamide 

Relevant academic research and scientific papers

Condensation of Schiff bases with 2-oxazolin-5-ones: simultaneous introduction of arylidene and amino moieties

Schiff bases condense with 2-oxazolin-5-ones having a C-4 methylene and/or C-2 methyl group, and the reaction in glacial acetic acid, containing freshly fused sodium acetate, produces 4-arylidene- and/or 2-styryl-2-imidazoline-5-ones as a result of simult

Condensation of 4-Benzylidene-2-methyloxazolin-5-one with Schiff Bases: Formation of 1-Aryl-4-benzylidene-2-styrylimidazolin-5-ones

Condensation of 4-benzylidene-2-methyloxazolin-5-one (II) with schiff bases (I) in acetic acid results in 1-aryl-4-benzylidene-2-styrylimidazolin-5-ones (III) and α-acetamidocinnamanilides (IV), characterised by spectral, analytical and chemical methods.