105199-35-7

Upstream product

• 74-96-4 ethyl bromide 
• 7569-26-8 chloromethyl p-tolylsulfone 
• 31378-03-7 1-phenyl-2-tosylethanone 
• 111895-33-1 2-tosyl-1-phenyl-1-butanone 
• 925901-20-8 2-chloro-1-phenyl-2-(toluene-4-sulfonyl)-butan-1-one 

Downstream Products

• 105199-31-3 8-Nitro-5-<1-(p-tolylsulfonyl)propyl>quinoline 
• 105199-21-1 3-Methyl-2-oxa-1H-1,7-phenanthroline-4(3H)-one 
• 105199-20-0 5-Nitro-8-<1-(p-tolylsulfonyl)propyl>quinoline 
• 105199-26-6 6-Nitro-2-<1-(p-tolylsulfonyl)propyl>quinoline 
• 108450-95-9 1-Nitro-4-(1-(p-tolylsulfonyl)propyl)naphthalene 
• 1071479-07-6 1,1,1-trifluoro-N-[(4-{1-[(4-methylphenyl)sulfonyl]propyl}phenyl)(oxido)(trifluoromethyl)-λ6-sulfanylidene]methanesulfonamide 
• 1071479-13-4 N-[(4-{1-chloro-1-[(4-methylphenyl)sulfonyl]propyl}phenyl)oxido(trifluoromethyl)-λ4-sulfanylidene]trifluoromethanesulfonamide 

Relevant academic research and scientific papers

Chemoselective mono halogenation of β-keto-sulfones using potassium halide and hydrogen peroxide; synthesis of halomethyl sulfones and dihalomethyl sulfones

The synthesis of α-halo β-keto-sulfones using potassium halide and hydrogen peroxide as a chemoselective mono halogenation reagent and the synthesis of α,α-symmetrical and asymmetrical dihalo β-keto-sulfones and α-halo, α-alkyl and β-keto-sulfones is described. Base induced cleavage of α-halo β-keto-sulfones, α,α-dihalo β-keto-sulfones, and α-halo, α-alkyl β-keto-sulfones afforded the corresponding halomethyl sulfones, dihalomethyl sulfones and haloalkyl sulfones.

Reactions of Organic Anions, 142. - Reactions of α-Chloroalkyl Sulfones with Nitronaphthalene Derivatives

1- and 2-nitronaphthalene derivatives react with the carbanions derived from chloromethyl p-tolyl sulfone and tert-butyl chloromethyl sulfone to give products of the vicarious nucleophilic substitution of hydrogen predominantly or exclusively in position