52809-71-9

Upstream product

• 3179-10-0 (E)-1-methoxy-4-(2-nitrovinyl)benzene 
• 108-98-5 thiophenol 
• 75-52-5 nitromethane 
• 123-11-5 4-methoxy-benzaldehyde 
• 3179-10-0 1-methoxy-4-(2-nitro-vinyl)-benzene 

Downstream Products

• 113934-91-1 2-(p-methoxyphenyl)-2-(phenylthio)-1-aminoethane 
• 113934-94-4 (E)-N-[2-(4-Methoxy-phenyl)-2-phenylsulfanyl-ethyl]-3-phenyl-acrylamide 
• 113934-93-3 N-[2-(4-Methoxy-phenyl)-2-phenylsulfanyl-ethyl]-benzamide 
• 54797-23-8 trans-N-[2-(4-Methoxy-phenyl)-vinyl]-benzamide 
• 175089-70-0 N-<2-(p-methoxyphenyl)-2-(phenylsulfoxy)-ethyl>-formamide 
• 175089-69-7 N-<2-(p-methoxyphenyl)-2-(phenylthio)-ethyl>-formamide 
• 2501-37-3 (E)-N-[2-(4-methoxyphenyl)ethenyl]formamide 

Relevant academic research and scientific papers

[bmim]OH-promoted one-pot, three-component synthesis of β-nitro sulfides in water

A task-specific ionic liquid, [bmim]OH, has been found to be a highly efficient catalyst for one-pot, three-component coupling of aryl aldehydes, nitromethane, and thiols for the synthesis of β-nitro sulfides in water. The main advantages of the present p

Straightforward and highly efficient catalyst-free regioselective reaction of thiol to β-nitrostyrene: a concise synthesis of vinyl sulfide and nitro sulfide

Under catalyst-free reaction conditions, solvent-mediated addition of thiol 2 to β-nitrostyrene 1 proceeded with regioselective control to afford either adduct 3 or vinyl sulfide 4 in good to excellent yield. Thermodynamic and autocatalytic reaction mecha

Synthesis of Some Naturally-occurring Styrylamides

Thermal elimination from N-(β-phenyl-β-phenylsulphinylethyl)amides yielded styrylamides (2)-(4).