Can hydrogen be abstracted from urea?

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Urea reacts with acids to form uronium ions, but its reaction with alkalis is less understood. Dissolving urea in NaOH raises questions about potential reactions and the possibility of hydrogen abstraction from the NH2 groups. Strong bases, such as lithium diisopropylamide (LDA) or lithium hexamethyldisilazide (LHMDS), may facilitate this abstraction, as indicated by the Bordwell pKa of urea at 26.9 in DMSO. The hydrolysis of cyanamide is noted as a reverse reaction in urea preparation, suggesting that strong bases are required for significant reactions. Overall, the discussion highlights the complexities of urea's reactivity with alkalis and the need for strong bases to achieve hydrogen abstraction.
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Homework Statement


Urea is known to react with an acid to form salt. The carbonyl oxygen of urea is protonated in the process to form uronium ion. But, I have not seen conclusive reaction of urea with an alkali. So, if urea is dissolved in NaOH, what are the possible reactions? Can hydrogen be abstracted from one or both NH2 group? What reagent can afford this abstraction if any.

Homework Equations


(NH2)2CO + HCl --> (NH2)2COH+ Cl-
(NH2)2CO + NaOH --> ?
(NH2)2CO + ? --> HNCONH2 ]-
(NH2)2CO + ? --> HNCONH ]2-

The Attempt at a Solution

 
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The reverse reaction, namely the hydrolysis of cyanamide is used in the preparation of urea. To reverse it, you will need a rather strong base. E.g. heating urea with metallic sodium.
 
You need to find pKa for these protons and then find a base strong enough. Definitely won't happen in water, and I doubt it will be possible to isolate such cations as salts, but organic chemists routinely use bases that should do the trick.

Edit: DrDu beat me.
 
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