31413-60-2

Upstream product

• 613-90-1 benzoyl cyanide 
• 56-23-5 tetrachloromethane 
• 98-88-4 benzoyl chloride 

Downstream Products

• 40920-42-1 3,3-dichloro-1,2-diphenylprop-2-en-1-one 
• 30698-30-7 methyl 2-cyano-2-phenylacetate 
• 27061-52-5 3,3-Dichlor-2-phenyl-acrolein 
• 27061-54-7 3,3-Dichlor-2-phenyl-acrylsaeure 
• 88703-73-5 (Z)-3-Chloro-2-phenyl-3-(p-tolylsulfonyl)acrylonitrile 
• 88703-71-3 (Z)-3-Chloro-2-methyl-3-(p-tolylsulfonyl)acrylonitrile 
• 40920-43-2 4,4-Dichloro-3-phenyl-but-3-en-2-one 
• 53366-83-9 4,4-Dichloro-3-phenyl-but-3-en-2-ol 
• 40920-44-3 1,1-Dichloro-2-phenyl-pent-1-en-3-one 
• 33128-45-9 1,1-Dichloro-2-phenyl-pent-1-en-3-ol 
• 40920-40-9 (E)-5,5-Dichloro-4-phenyl-penta-2,4-dienoyl chloride 
• 40920-46-5 3-chloro-2-phenyl-1-indenone 
• 40920-39-6 5,5-Dichlor-4-phenyl-4-penten-2-insaeure 
• 40920-48-7 (Z)-2-Bromo-5,5-dichloro-4-phenyl-penta-2,4-dienoic acid 

Relevant academic research and scientific papers

One-pot four-component synthesis of 2-aryl-3,3-dihaloacrylonitriles using potassium hexacyanoferrate(II) as environmentally benign cyanide source

An efficient route to one-pot four-component reactions of aroyl chlorides, potassium hexacyanoferrate(II), triphenylphosphine and carbon tetrahalides to synthesize 2-aryl-3,3-dichloroacrylonitriles and 2-aryl-3,3- dibromoacrylonitriles was described. This