81358-61-4

Upstream product

• 30058-54-9 α-dichloromethyl phenylsulfoxide 
• 1193-82-4 racemic methyl phenyl sulfoxide 
• 945982-99-0 4-benzenesulfinyl-4,4-dichloro-3-methyl-1-phenylbutan-1-one 
• 13735-81-4 1-styrenyloxytrimethylsilane 
• 69753-43-1 1-chloro-1-phenylthio-2-propanone 

Downstream Products

• 945983-25-5 C₁₇H₁₄O₂S 
• 39517-83-4 4-methyl-2-phenylfuran 

Relevant academic research and scientific papers

Selective Reaction of Silyl Enol Ethers with α-Chloro-sulphides containing a Ketone Group

Reaction of silyl enol ethers (1) with α-acyl-α-chloro-sulphides (2; n = 0) gives furans (4), whereas with β- or γ-acyl-α-chloro-sulphides (2; n = 1 or 2) diketones (3) are obtained.

A short synthesis of highly substituted furans from alkenyl aryl ketones with dichloromethyl phenyl sulfoxide

Two-step synthesis of 2-aryl-5-(phenylsulfanyl)furans was achieved starting from alkenyl aryl ketones and dichloromethyl phenyl sulfoxide. The phenylsulfanyl group was successfully converted to other functional groups, via sulfinyl group, to give highly substituted 2-arylfurans in good overall yields.