From: Darren Rhodes (darren.rhodes$##$gmail.com)
Date: Thu Nov 15 2007 - 09:06:57 EST
No. In relation to your question below: does the reaction go to
comletion? I've ran systems where I attempt to oxidise a secondary
alcohol to a ketone but the reaction didn't go to completion
irrespective of the number of molar equivalents of oxidant.
Has anyone else observed this phenomenon and if so, do you have a rationale?
Darren.
On 05/11/2007, ricardo mendonca <ricfmendonca$##$gmail.com> wrote:
>
> Hi
>
> As anyone run into unwanted chlorination during a Sodium Hypochlorite
> (NaClO; BLEACH) oxidation of a secondary alcohol to a ketone?
> If yes, have you used any chlorine scanveger? Which one?
> References of articles are well apreciated.
> I am aware of the use of chlorine scanvegers (2-methyl-2-butene, and alike)
> during the Sodium chlorite (NaClO2) oxidation of aldehydes to carbox. acids.
> I wonder if anyone have used sulphamic acid (chlorine scavenger) in this
> reactions and if it did inhibit chlorination issues.
> Thanks in advance
>
> Ricardo Mendonca
>
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