40888-37-7

Upstream product

• 107905-41-9 N-(2,2,2-trichloro-1-hydroxyethyl)-p-chlorobenzenesulfonamide 
• 81924-15-4 N-(2,2,2-trichloroethylidene)-4-chlorobenzenesulfonamide 
• 17260-65-0 N,N-dichloro-4-chlorobenzenesulfonamide 
• 40888-36-6 C₈H₆Cl₅NO₂S 

Downstream Products

• 1430086-44-4 4-chloro-N-(prop-2-yn-1-yl)-N-(2,2,2-trichloroethyl)benzenesulfonamide 
• 1430086-42-2 4-chloro-N-(prop-2-en-1-yl)-N-(2,2,2-trichloroethyl)benzenesulfonamide 

Relevant academic research and scientific papers

Sulfonamidation of halogen-substituted electrophiles with N-(2,2,2-trichloroethyl)arenesulfonamides

Reactions of N-(2,2,2-trichloroethyl)arenesulfonamides with primary alkyl bromides and iodides, allyl bromide, chloroacetonitrile, and benzyl chloride in acetonitrile on heating in the presence of potassium carbonate gave the corresponding N-alkyl-N-(2,2,2-trichloroethyl)arenesulfonamides.

Reduction of N-(Polychloroethylidene)- and N-(1-Hydroxypolychloroethyl) arenesulfonamides with adamantane in the presence of superacids

N-(2,2,2-Trichloroethylidene)-, N-(2,2-dichloro-2-phenylethylidene)-, and N-(1-hydroxy-2-polychloroethyl) arenesulfonamides reacted with adamantane in carbon tetrachloride in the presence of oleum or concd. H2SO 4-P4O