4773-36-8

Upstream product

• 611-73-4 Benzoylformic acid 
• 81265-15-8 methyl 2,2-dichloro-2-phenylacetate 
• 61031-72-9 dichlorophenyl-acetic acid 
• 103-80-0 phenylacetyl chloride 

Downstream Products

• 19450-46-5 2,2-Dichloro-N-(octahydro-naphthalen-4a-yl)-2-phenyl-acetamide 
• 91767-82-7 N,N-Diethyl-2,2-dichloro-phenyl-acetamid 
• 13027-91-3 2,2-Dichlor-phenylessigsaeure- 
• 112439-83-5 2,2-Dichlor-2-phenylacetomorpholid 
• 80608-18-0 1,1-Dichlor-4-(N-methylanilino)-1-phenyl-3-butin-2-on 
• 105066-14-6 2,2-Dichlor-2,N,N-triphenylacetamid 
• 115592-64-8 N-Benzyl-2,2-dichlor-N-methyl-2-phenylacetamid 
• 197857-86-6 N-allyl-N-benzyl-2,2-dichloro-2-phenylacetamide 
• 115592-39-7 N-Benzyl-N-methyl(2-phenylethinyl)amin 
• 115592-46-6 2-(N-Methylbenzylamino)-3-phenyl-5-(p-tolylsulfinyl)furan 
• 112439-85-7 N-(1,2-Dichlor-2-phenylvinyl)morpholin 
• 112439-84-6 N-(1,2-Dichlor-2-phenylvinyl)morpholin 
• 105066-10-2 N-phenyl-N-(phenylethynyl)aniline 
• 105066-15-7 (E,Z)-N-(1,2-Dichlor-2-phenylvinyl)-N-phenylanilin 

Relevant academic research and scientific papers

Breakthrough in the α-perchlorination of acyl chlorides

The preparation of -perchloroacyl chlorides, from reaction of the corresponding unfunctionalized acyl halides with chlorine, was efficiently achieved under base-catalysis, using a tetraalkylammonium chloride as catalyst. The process is solvent-free and th

Halogen atom transfer radical cyclization of N-allyl-N-benzyl-2,2-dihaloamides to 2-pyrrolidinones, promoted by Fe0-FeCl3 or CuCl-TMEDA

The halogen atom transfer radical cyclization of a N-allyl-N-benzyl-2,2-dihaloamides to 2-pyrrolidinones has been carried out in high yields under mild conditions, in a reaction promoted by CuCl-TMEDA or Fe0-FeCl3 in acetonitrile or N,N-dimethylformamide, respectively.