Answer to Question #27073 in Inorganic Chemistry for farzaneh hamedi

Question #27073
Hello.I have synthesed an imidazolil ring that on this ring I have 2 aryle groups.one of them is aldehydel and the other is methyl sulfid.in which way I can change sulfid to sulfonyl group(oxidation)without influencing on aldehyde group?(I need something that speacially oxid ONLY sulfide)if you can help me and introduce somethin that can do this reaction,I will be so thankfull
1
Expert's answer
2013-04-03T11:03:25-0400
Under the effect of mild oxidant (hydrogen peroxide in acetone or glacial acetic acid, peracids) sulfides are oxidized to sulfoxides:
CH3SH + H2O2 CH3SOH
the action of energetic oxidants (potassium permanganate, nitric acid) oxidation is to sulfones:
CH3SOH + H2O2 CH3SO2H
These reactions are used as a preparative method for the synthesis of sulfoxides and sulfones. In your case, you can try to oxidize 60% peroxide in acetone. Imidasol ring stand, and the aldehyde group will remain intact.

Need a fast expert's response?

Submit order

and get a quick answer at the best price

for any assignment or question with DETAILED EXPLANATIONS!

Comments

No comments. Be the first!

Leave a comment

LATEST TUTORIALS
APPROVED BY CLIENTS