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Author: Subject: Sulfonation Of Phenol
Vlassis
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[*] posted on 22-5-2012 at 06:27
Sulfonation Of Phenol


The other day I was reading an article concerning the synthesis of catechol by reacting molten potassium hydroxide with orthophenolsulfonic acid.I was wondering if the reaction is even possible, since the difference between melting points of those two compounds is around 250 degrees.I could not find the exact reaction somewhere, so I thought it might be this:


gasdasdg a.PNG - 11kB
I forgot a 2 in front of the potassium hydroxide

[Edited on 22-5-2012 by Vlassis]
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barley81
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[*] posted on 22-5-2012 at 06:34


Arylsulfonic acids react with molten alkali by forming alkali phenoxides and sulfites. Hydrogen gas is not produced. Typically, an alkali sulfonate salt is used instead of the sulfonic acid.

ArSO<sub>3</sub>K + 2 KOH -> ArOK + K<sub>2</sub>SO<sub>3</sub> + H<sub>2</sub>O

Hypothetical reaction of the dipotassium salt of o-phenolsulfonic acid and KOH equation:

C<sub>6</sub>H<sub>4</sub>SO<sub>4</sub>K<sub>2</sub> + 2KOH -> C<sub>6</sub>H<sub>4</sub>(OK)<sub>2</sub> + K<sub>2</sub>SO<sub>3</sub> + H<sub>2</sub>O

Check Vogel's Practical Organic Chemistry in the SM library for more information on arylsulfonic acids and fusion of their salts with alkali. I'm not sure if the compound you mention is a special case.

[Edited on 22-5-2012 by barley81]
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Vlassis
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[*] posted on 22-5-2012 at 07:13


Thank you for your reply.I will check out Voguel, but do you know any possible synthesis of the ortho and not the para sulfonic acid.I know that you must keep the temperature low, but how low exactly?And after that, how to seperate the ortho para and meta sulfonic acids formed?
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leu
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[*] posted on 22-5-2012 at 15:54


From Thorpes Dictionary of Applied Chemistry:

Pyrocatechol may be obtained in a pure condition by fusing one mole of phenol ortho sulphonic acid with twenty four moles of caustic potash at 320 to 330 degrees Celsius. The yield is twenty percent of the theoretical.

:cool:




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