70509-10-3

Upstream product

• 64-17-5 ethanol 
• 126737-52-8 N,N-diethyl-N-methyl-4-phenyl-3-aza-3-butenylammonium iodide 
• 100-52-7 benzaldehyde 
• 23956-51-6 N¹-benzylidene-N²,N²-dimethylethane-1,2-diamine 
• 1749-16-2 N'-(benzylideneamino)-N,N-diethylethan-1-amine 
• 70509-19-2 N‐(2‐chloroethyl)‐1‐phenylmethanimine 
• 70509-12-5 1-phenyl-3-methoxy-2-aza-1-butene 
• 70509-11-4 1-phenyl-2-aza-1,3-butadiene 

Downstream Products

• 70509-12-5 1-phenyl-3-methoxy-2-aza-1-butene 
• 5281-18-5 benzaldehyde, hydrazone 
• 13880-55-2 N,N,N',N'-tetramethyl-C-phenylmethanediamine 
• 6425-08-7 4,4'-(phenylmethylene)bismorpholine 
• 119136-04-8 3-(diethylamino)-1-phenyl-2-aza-1-butene 
• 119136-05-9 1-phenyl-3-piperidino-2-aza-1-butene 
• 119136-06-0 1-phenyl-3-morpholino-2-aza-1-butene 
• 622-29-7 N-Benzylidenemethylamine 
• 5292-53-5 diethyl benzalmalonate 
• 588-64-7 benzaldehyde phenylhydrazone 

Relevant academic research and scientific papers

SYNTHESIS AND SOME TRANSFORMATIONS OF 1-ARYL-2-AZA-1,3-BUTADIENES

The synthesis of 1-aryl-2-aza-1,3-butadienes was realized by the alkaline cleavage of diethylmethyl(4-aryl-3-aza-3-butenyl)ammonium iodides or by the dehydrochlorination of 1-chloro-4-phenyl-3-aza-3-butene.They react with alcohol at the terminal vinyl group.The direction of reaction with amines depends to a large degree on the nature of the nucleophile.