UranylPeroxysulfate
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Aminoguanidine bicarbonate from urea, P2O5, and hydrazine
I’m working on the synthesis of aminoguanidine bicarbonate. The synthesis requires a source of cyanamide, which is usually provided by calcium
cyanamide from heating calcium cyanate to 900C. However, a temperature of 900C is unobtainable for me. So, I plan to synthesize aminoguanidine
bicarbonate the following way instead:
1. Mix stoichiometric amounts of urea and P2O5, and then heat the mixture to the melting point of urea (135C) to dehydrate urea to cyanamide
phosphate.
2. Neutralize the phosphoric acid with NaOH
3. Add hydrazine sulfate, adjust the pH, and make aminoguanidine bicarbonate as usual (same as the calcium cyanamide method, except filtering CaSO4 is
no longer needed)
I attempted steps 1 and 2, but when I tested the mixture for cyanamide using AgNO3 in ammonia, it came out negative. Any idea what went wrong? I was
thinking that perhaps the cyanamide got destroyed in the reaction or the phosphate caused the AgNO3 to precipitate as silver phosphate (and is this no
longer available to react with cyanamide).
If something does work, sulfonate it.
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Boffis
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@Uranylperoxysulfate. I wouldn't bother making calcium cyanamide, it is easily bought. I don't know where you are based but in Europe it is easily
available at garden shops and agricultural suppliers e.g.:
https://gro-welldirect.co.uk/growing-media/soil-conditioner/...
And at just over £1 a kg you can't go wrong. I am currently working on preparing cyanamide from it for other purposes using the acetic acid-ether
extraction route. I am currently away from my lab so work has ground to a holt for now but I have run a few small scale experiments. The key issue is
knowing how much acetic acid is required because you must have a small excess. I have a paper that describes the process somewhere.
Edit.
I am not sure you can dehydrate urea to cyanamide because the cyanamide would polymerise almost immediately under ether acid or basic conditions. To
make urea react with hydrazine you must must first convert it to an O-alkyl-isourea salt. This is possible with dimethyl sulphate and similar reagents
but generally the isourea salts are prepared from cyanamide. I have references on most of these procedures but they are not easy for amateurs.
If you search this forum there are procedures for the direct conversion of crude calcium cyanamide and hydrazine salts into aminoguanidine
bicarbonate.
[Edited on 21-5-2021 by Boffis]
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UranylPeroxysulfate
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@Boffis. Thanks for the information. Unfortunately, it is pretty much impossible to buy calcium cyanamide of any form in China (where I live). I can
buy dicyandiamide quite easily though. Is it possible to make aminoguanidine bicarbonate from it?
Polymerization is definitely an issue with cyanamide. I know for certain that it dimerizes in basic conditions, but I couldn't find any information
about it polymerizing in acid, especially weak ones like phosphoric acid. Considering your cyanamide didn't polymerize when you add excess acetic acid
to it, I doubt polymerization is the issue.
Making an O-alkyl-isourea salt is not a problem for me. I have some benzyl chloride leftover from my Grignard reaction experiments; it should alkylate
urea quite well. Could you give me the reference for the procedures?
If something does work, sulfonate it.
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clearly_not_atara
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I agree with Boffis -- I doubt that throwing dehydrating agents at urea is likely to produce any cyanamide. Maybe some interesting semiconducting
polymers, though.
Bakibaev and Shtrykova (attached) seem to suggest that conversion to the iodide and rxn in neutral (not basic) media at about 100 C would be a good
strategy, but they don't give many details.
Attachment: bakibaev1995.pdf (770kB)
This file has been downloaded 429 times
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Boffis
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Cyanamide is only stable in the presence of acetic acid at low temperature ie <20 C. Furthermore strong dehydrating agents convert urea to triazine
derivatives like melamine in a single step. There is a rather old monograph on urea (ACS I think), a bit out of date now but worth reading; the facts
haven't changed only the interpretations. This book discusses numerous attempts (all unsuccessful) to prepare cyanamide from urea.
Here are the papers I was referring to:
Attachment: O-Methylation of urea to methyl isourea JCS Werner 1914.pdf (142kB)
This file has been downloaded 397 times
Attachment: Preparation of O-Alkyl iso-urea TransRSNZ Ongley 1948.pdf (185kB)
This file has been downloaded 383 times
There are some interesting references in the paper supplied by clearly-not-atara, particularly No.8 by C. D. Nenitzescu which deal with the use of
alkyl iodides and urea.
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