Chemical Forums
Chemistry Forums for Students => Organic Chemistry Forum => Topic started by: jmarjorie on July 04, 2005, 07:14:40 AM
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Hi everybody,
Is there any simple way in the lab to convert Tri Chloro isoCyanuric Acid (TCCA) to its lesser derivative Sodium DiChloro IsoCyanuric acid (NaDCIC) ?
This will involve the removal of 1 atom of chlorine and the addition of sodium in its place. It's baffled me.
Thanks in advance,
jmarjorie
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You might be able to do it with Na0, but it's probably be messy.
Possibly also with something like NaHMDS.
Maybe also try reducing with n-Bu3SnH to form the dichloro compound and then just deprotonate.
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urm, basically what Mr. Movies said, take the dichloro compound, deprotonate with NaOH.
Btw, how fair is to call thi-chloro compund an acid - after all, it isn't a Bronsted acid anymore.