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Chris The Great
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[*] posted on 25-11-2005 at 23:26
Nitramide reactions


Some ideas occured to me recently, about using nitramide to prepare interesting and powerful energetic materials.

I haven't been able to find much information to confirm whether my ideas would or would not work however, except the abstract of a journal (see below).

The first idea was to synthesis HANA (hexaazahexanitroadamantine), C4H4N12O12, which has a density of 2.10 g/cc. In this case the reaction would be:
6NH2-NO2 + 4CHI3 -> C4H4N12O12 + 12HI
The HI would most likely have to be absorbed by a base, ie triethylamine, that will not decompose nitramide rapidly. I would think the high reactivity of the C-I bonds would allow this reaction to take place readily. On the other hand the probable strain of the molecule would make the reaction disfavourable. They might also react to form other products, and not form HANA at all.
So, I am not really sure whether that would work, if it did it would be quite easy to do at home and would produce a very interesting energetic material.

The second one would be reacting nitramide with glyoxal, to form a piperidine ring NO2-N(CH(OH)-CH(OH))2N-NO2. This would no doubt lend itself well to the synthesis of some interesting energetics.
The original compound I had in mind that could be made from it was HHTDD, which would be formed by condensing the above compound with dinitrourea, adding a dinitrourea group on each side and eliminating water. Since water would decompose the DNU, would would have to form the tetracetyl of the nitramide product, and react that with the DNU instead as acetic acid would form, and it will not hydrolysis the DNU.
HHTDD has a densitry of 2.07 g/cc, perfect O balance, and is considered to be the most powerful explosive known. However, the nitration conditions require large amounts of 100% HNO3 and N2O5 and so straight synthesis would be difficult.
If nitramide forms the wanted ring, then the only starting materials are acetic anhydride, dinitrourea, glyoxal and the appropriate solvent, and maybe a catalyst.

The evidence I have for nitramide reacting with aldehydes comes from a journal abstract I came across while searching to see if these ideas would work, in which nitramide and formaldehyde formed a stable and powerful polymer.
A Study on the Condensation of Nitramide (NH2NO2) with Formaldehyde and the Characteristics of the Products Formed
Z. Raszewski, M. Syczewski
Propellants, Explosives, Pyrotechnics
Volume 24, Issue 6 , Pages 366 - 370

It would be nice if someone got it, the polymer looks like it would be interesting on it's own.
(CH2N-NO2)n --> nCO + nH2O + nN2

I have attached drawings of HANA, NO2-N(CH(OH)-CH(OH))2N-NO2 (not sure of the name) and HHTDD so it is much clearer what I am talking about.

Thoughts?

nitramide.gif - 5kB
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tom haggen
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[*] posted on 26-11-2005 at 00:48


That is a massive amount of gass molcules:P



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chemoleo
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[*] posted on 26-11-2005 at 08:49


Nice ideas:)

Your HANA, do you have a reference on this?
Iodoform and nitramine - sounds simple enough. Do you have decent references on the production of H2N-NO2? I thought it was notoriously unstable.
I imagine getting the final product would be difficult as the proportions have to be gotten exact. How would you avoid getting intermolecular crosslinks, rather than this caged structure?
The reaction of the C-I moiety with H-NR2 would require conditions generally used for N-alkylations (similar to what was asked in the novocaine thread).

On the second one, I guess you got the idea from the tetranitropiperazine, which was described in one of the PEP papers by this Munich group (Klapoetke)?
I suppose this could work, they use formamide as opposed to nitramide.
Nitrating this is gonna be a pain or two, nonetheless (TFAA and such).

Re. these polymers - I had similar ideas like that before. For instance, I condensed CH2O with guanidine BASE, and very soon after, a white plasticky substance formed.
Of course this could now be modified to use nitroguanidine, nitro urea, and so on, and possibly make the nitrate salt of this afterwards. Alternatively one could start playing with semicarbazide, or aminoguanidine, and so on. So many things to do!




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Chris The Great
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[*] posted on 26-11-2005 at 20:00


No reference on the HANA, just popped into my head one day. So I have no clue if it will actually produce the wanted product, though I am sure they will react to produce high nitrogen content compounds.

Second one also popped into my head, though nitrating to the tetranitro was inspired by that. But the main idea behind it would be an easy production of HHTDD without having to go through a difficult nitration process, which seems to be the main problem behind making it. I read about HHTDD long before I heard that the precursor could also be nitrated to a powerful explosive as well. It them occured to me that since the end nitrogens on the molecule are the ones the require the difficult nitration conditions, it would be possible to condense with dinitrourea rather than urea and remove the need for the harsh nitration conditions. Then, I thought of using nitramide instead of formamide, and not needing any nitration at all. Seemed like something worth sharing.

Nitramide is produced from hydrolysis of dinitrourea, which proceeds immediatly upon addition to water. I am not sure what yields are after extracting, although it may not even be necessary and the solution of nitramide formed might be possible to use directly in the procedures.
It fits well with using it to form HHTDD, since it will be formed from DNU, and then DNU is used again to make the HHTDD. Dinitrourea is made by a straightforward nitration of urea, however it is very impure and rapidly breaks down if not washed with trifluoroacetic acid after the nitration (other solvents probably work but haven't been revealed yet). Yields are around 75% or so, and it may not need to be washed if it is just hydrolysed after the synthesis to make nitramide.
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The_Davster
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[*] posted on 26-11-2005 at 21:35


Definatly interesting, I think the HANA reaction is pretty likely if the C-I with H-N is able to take place in the standard way. There is actually very little strain in this molecule, after all it is (figurativly) a bunch of cyclohexane rings. Since cyclohexane pretty much has a strain of zero, the strain on this molecule is only slightly greater. I made this molecule with a molecular kit and there was only very mild forcing of the last bond together(unlike cubane which snapped the sp3 carbon when making the molecule).

Compared with what else could theoretically form based on the reaction of just the C-I and H-N, such as cyclobutane rings in the same format as the adamantane structure, and cyclononane based structures, and even larger, ring strain reaallly favours the adamantane structure.

Hehe...use iodopicrin instead of iodoform, :o;)....4 more nitros on the molecule:D




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[*] posted on 26-11-2005 at 23:57


Quote:
Originally posted by Chris The Great
A Study on the Condensation of Nitramide (NH2NO2) with Formaldehyde and the Characteristics of the Products Formed
Z. Raszewski, M. Syczewski
Propellants, Explosives, Pyrotechnics
Volume 24, Issue 6 , Pages 366 - 370


For whatever reason I found that on my desktop, forget what I was thinking when I got it. I put one on nitrourea -> nitramide in the zip as well.

I think anyone can open PEP articles from between 1998-2002 through wiley, and they are all downloadable on one of the ftp's.

http://www3.interscience.wiley.com/cgi-bin/fulltext/5008392/...

That opens ... right? click the "PDF" link.

[Edited on 27-11-2005 by Axt]

Attachment: nitramide.zip (848kB)
This file has been downloaded 798 times

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PHILOU Zrealone
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smile.gif posted on 20-12-2005 at 11:38


1)Exchange hability of iodine from CHI3 is much lower than from CI3-NO2....To play with NH2-NO2 is a good idea but in the hypothetical point of view HI will be formed..HI is strong acid and reducer...so chances of NH2-NO2 to survive which are already low will be even lower....but who knows...trial doesnt cost much...
To overcome this HI problem ... it must be possible to use Ag-NH-NO2 in a way to drive the reaction to the good side without the annoying acid effect...
O2N-CI3 + 3 Ag-NH-NO2 --> O2N-C(NH-NO2)3 + 3AgI...
Being bounded so the resulting molecule (maybe very prompt to hydrolyse) must be a very strong acid...

So silver salt might be formed a second time...

O2N-C(NH-NO2)3 +3/2 Ag2CO3--> O2N-C(AgN-NO2)3 + 3/2 CO2 + 3/2 H2O
The later then reacted in the same fashion as the first time will give plannar polymer or the caged adamantane sphere you imagined but with nitros on each top...what is in favour of the spherisation or of the plannification of your multimeric coupound.

2)The second molecule you named HHTDD is indeed powerful and many trials have proven the cyclisation between O2N-N(CHOH-CHOH)2N-NO2 and DNU is very hard owing to the fact the two HO points in different directions...so it is very hard to get them to react 2 by two to get a first stressed pentaring and then a second one.
Thus the presence of the NO2 on the initial core molecule is a disavantage since they tends to improve chair shape instead of the boat you must have to allow easier cyclisation.

One possibility but I don't see how to get there...is to start from:
O2N-N(CI=CI)2N-NO2 (planar with I external in the plane)+2 (AgN(NO2))2C=O....you then possibly end up with the squeletton you asked but with two more insaturations...and nearly perfect planarity....

Another possibility would be to bend the initial molecule by bridging the two external Ns...bridge must be extractible once reaction is achieved without destroying the two others made rings...and also exchanged for NO2...

[Edited on 20-12-2005 by PHILOU Zrealone]




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Chris The Great
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[*] posted on 20-12-2005 at 20:38


Quote:
Originally posted by PHILOU Zrealone
2)The second molecule you named HHTDD is indeed powerful and many trials have proven the cyclisation between O2N-N(CHOH-CHOH)2N-NO2 and DNU is very hard owing to the fact the two HO points in different directions...so it is very hard to get them to react 2 by two to get a first stressed pentaring and then a second one.
Thus the presence of the NO2 on the initial core molecule is a disavantage since they tends to improve chair shape instead of the boat you must have to allow easier cyclisation.


Hmm, what are the sources here? I'm curious because the same molecule (with CHO instead of NO2) reacts readily with urea to form the wanted molecule, so I expected the reaction with DNU would also occur easily.


You are correct about HI reducing the NO2 groups, I didn't think about it but it is a possible side reaction that could occur quite easily and destroy the final product. Would it still happen if the HI is removed by a base? I would imagine that the reaction would at least be reduced drastically, but unfortunately it adds cost and complexity to the reaction.
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PHILOU Zrealone
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[*] posted on 21-12-2005 at 02:48


Quote:
Originally posted by Chris The Great
Hmm, what are the sources here? I'm curious because the same molecule (with CHO instead of NO2) reacts readily with urea to form the wanted molecule, so I expected the reaction with DNU would also occur easily.

:( Unfortunately I don't have readily acces to my books and notes(everything is in cardboard boxes for two years now-new mother's appartement, buildingwork, and now I go live with my girlfriend )...maybe in two weeks I wil be able to answer your question...
Regarding your -CH=O instead NO2...I wonder how do you account for the fact urea doesn't react with -CH=O?

Quote:
Originally posted by Chris The Great
You are correct about HI reducing the NO2 groups, I didn't think about it but it is a possible side reaction that could occur quite easily and destroy the final product. Would it still happen if the HI is removed by a base? I would imagine that the reaction would at least be reduced drastically, but unfortunately it adds cost and complexity to the reaction.

I guess this would be a solution...the base would activate the exchange of I...by scavenging the HI as soon as it forms...Of course the use of nitramine salts...is precisely a bit the same idea but under another form...
NH2-NO2 + OH(-) --> NH(-)-NO2 + H2O
CH3-I + NH(-)-NO2 --> CH3-NH-NO2 + I(-)

So if you also use the precipitation as a guiding line...
Silver is used as typical example for nucleophilic substitution of I but it is possible with other metals...
AgNH2-NO2 + CH3-I --> CH3-NH-NO2 + AgI
Also salts of nitramides are chemically stabler than the parent nitramide with regards to hydrolysis...




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Chris The Great
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[*] posted on 21-12-2005 at 16:43


Quote:
Originally posted by PHILOU Zrealone
Regarding your -CH=O instead NO2...I wonder how do you account for the fact urea doesn't react with -CH=O?


You are misunderstanding what I have in mind. I've attached a diagram of what reaction works, and what I have proposed using DNU. OAc is used because otherwise the water produced by the reaction would destroy the DNU. In the first reaction, the CHO is hydrolysed during the reaction.
It may need other incentives to get the reaction to proceed fully however, ie basic enviroment etc.

HHTDD.gif - 7kB
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[*] posted on 26-12-2005 at 08:23


greetings Philou

The second reaction in the last attachment is possible. One majour drawback, the first molecule (tetraacetyl dinitro derivative) is extremely hard to synthese.

The existance of AgNH-NO2 is under question.
"...trial doesnt cost much..."

Oh, it does...
High-tech laboratory complex is needed to experiment with cyclic nitramines. NMR and IR are out of question. 100% HNO3 is pain in the ass (the toxic effects on the lungs may be hidden for weeks !!!!!!!!!!!!!!!!!!!!!!!!).
I thought a "normal" fume hood will save me from NOx when working with liters HNO3... Wrong - you can smell it! A gas mask is also needed for full protection.
(accessible antidots for H(NOx) - immediately - ammonia (carefully breathe 3 times - 10seconds each) , second vitamine C (500mg immediately - 3x200mg per day - 5 days, then 3x100mg 20 days (from a military tox book)
P2O5 mixed with HNO3 is another trouble , igniting everything it falls on. Acetic anhydride mixed with c.HNO3 is a high explosive on itself (it could be high, primary, or just burn - depending on accidental conditions) .



There is no problem to make - medina for example - in BAD equipped lab, but more complex thing is very problematic.




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[*] posted on 26-12-2005 at 08:28


The diagram looks fine. I don`t know the reaction works esay with HCL. Rather than with a other solution or the way from a existing nitramide to a nitramin ?
It have likely better attributes (density ad VOD) as TNGU and DNGU.

I have attached a diagram to get a THD (Tetrahedran) nitramin or nitramide derivat maybe with the same way, but diagram not uploadable :( ?

The formulas here.

(NNO2)3CNO2
(NHNO2)3CNHNO2

[Edited on 26-12-2005 by Madandcrazy]
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[*] posted on 14-6-2006 at 09:23


Quote:

High-tech laboratory complex is needed to experiment with cyclic nitramines.


I belive N2O5 is hard to get, when so ever. You don`t can nitrate higher when the N2O5/HNO3 mix is not available.

Is N2O5 available by homemade, dehydration of HNO3, ammonium nitrate etc. ?

[Edited on 14-6-2006 by Mason_Grand_ANNdrews]
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[*] posted on 15-6-2006 at 05:00


N2O5 is very instable, afaik you can not store it in the pure form.
P2O5+HNO3 yields N2O5 and HPO3.
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[*] posted on 15-6-2006 at 08:27


N2O5 is stable at -10 gegree celsius and very hycroscopic.

Your knowledge are correct, N2O5 was easiest avialable by HNO3 and P2O5 ?

I`ve found a articel, N2O5 was manufactured per distillation.
Fuming white HNO3 ;) is destilled with ozon gas to a beaker with freshly prepared P4O10 which was cooled to -10 gegree celsius and N2O5 should formed in a oxidation process when the ozonylized HNO3 passed to the P4O10.

I belive P4O10 is available as a drying agent for the industrie and is formed by the oxidation of phosphors with a lage excess of oxygen.
P4 + 5 O2 -> P4O10

P4O10.bmp - 29kB
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[*] posted on 5-3-2012 at 12:32


I do not think "HANA" could be made. The chemistry of formic acid, for example, is very different from that of formaldehyde. I am not sure the best way to explain this. Certainly, HANA could not be made by simply using formic acid instead of formaldehyde in the usual RDX process. N-nitroformamide, NO2-NH-CH=O, might form, but there could not be any further condensation. Amides are very stable and usually relatively unreactive because the amine group is electron donating to the oxygen atom.

So one might speculate what would result from condensing bromoform with nitramide. First it should be mentioned that iodoform is probably not the best regent to use, because the condensation will produce hydrogen iodide, which is a strong reducing agent, and could potentially reduce the nitramine groups. This would not be a problem in aqeous solution, since it is only anhydrous HI that is a very reactive reducing agent. But in the presence of water, the intermediate products of condensation (between CHBr3 and NH2NO2) are likely to be immediately hydrated, forming N-nitroformamide. So back to the idea of using bromoform, I still think "HANA" would be unlikely to form.

The initial intermediate product that would form would be
Br-CH=N-NO2
But think about what would immediately happen. The bromine atom would have a tendancy to immediately ionize off, because there is a nitrogen atom also bonded to the carbon. This could actually be a very complicated reaction, and I would not know exactly which mechanism it would proceed through. But this intermediate would likely not be chemically stable, and would decompose before it had a chance to condense with another nitramide.

A related question would be what results from the bromination (in the absence of water) of RDX. Could this form bromo-RDX? No, I think this is unlikely. There would instead be other degredation products.
http://www.sciencemadness.org/talk/viewthread.php?tid=908

Quote: Originally posted by BASF  
I wonder wether it would be possible to brominate RDX...
Mild conditions. The problem is, i know few to nothing about nitramine-chemistry.....


Quote: Originally posted by PHILOU Zrealone  
halogenation of RDX might work but as you said the C-N link might not survive the halide.

(-CHX-N(NO2)-)3 where X = F, Cl, Br or I
Those haloRDX are also interesting because they might be precursor for couplage reactions of other explosophoric groups.

Maybe a different way of action must be investigated!
CH3-O-CH=O + NH2-NO2 --> CH3-O-CH=N-NO2
3CH3-O-CH=N-NO2 --> (-CH(OCH3)-N(NO2)-)3
(-CH(OCH3)-N(NO2)-)3 +3 HBr(g) --> (-CH(OH)-N(NO2)-)3 + CH3Br(g) or (-CHBr-N(NO2)-)3 + CH3OH


chloroform typically reacts with organic amines to form isocyanides. "chloroform heated with an excess of n-butylamine yield the same sub- stance along with n-butyl isocyanide and unidentified material"

So [-]C Ξ N[+]—NO2 might be expected to form as the intermediate product, which would likely spontaneously polymerise to and degrade. Trinitro-1,2,3-triazine, for example, has never been isolated.

Note that [-]C Ξ N[+]—NO2 is not "nitromethanenitrile", which has the formula
NΞC—NO2

[Edited on 5-3-2012 by AndersHoveland]
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