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Author: Subject: DMSO + Br2 -> ???
Protium
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[*] posted on 1-1-2005 at 03:15
DMSO + Br2 -> ???


What does one get when bromine reacts with dimethylsulfoxide?

I tell you this product (?) has got to be the nastiest smelling stuff I've ever personally encountered.

The only thing that I can figure is that the Br attacks/replaces a H on the methyl group possibly similar to a bromoacetone formation. I'm not sure if there is any tautoterism involved with the sulfoxide group as in the keto/enol group.

Also there was a bit of HBr necissarily present during the in situ production of Br2 from NaBr and H2SO4. I don't know if this impacted the end product either.

Any clues?




It just depends on how you look at it...
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BromicAcid
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[*] posted on 1-1-2005 at 05:30


Quote:
Bromination of DMSO with elemental bromine leads to the formation of trimethylsulfonium bromide. Methanesulfonic acid, paraformaldehyde, dimethyl disulfide, and hydrogen bromide are formed as byproducts.

CH3SOCH3 --(Br2)--> (CH3)3S+Br- [75%]

From 'Technical Bulletin Reaction Solvent Dimethyl Sulfoxide (DMSO)' Gaylord Chemical Corporation




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