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Nicodem
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Excellent find, thanks Klute!
I don't know what practical use could such a reaction have, but this is the first paper I saw that describes good to excellent yields in N-oxidation
of R-CH2-NH2 type of amines to nitro compounds.
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sonogashira
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The reference was actually posted by quantum_dom in the very first post of this thread, though i guess he didn't have access to the paper.
Nicodem: "this is the first paper I saw that describes good to excellent yields in N-oxidation of R-CH2-NH2 type of amines to nitro compounds."
Here's another one (also given in the first post! The others concern oxidation of aromatic amines) using isomers of butylamine:
Attachment: Nitroalkanes from Amines with DMDO.pdf (119kB)
This file has been downloaded 1250 times
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Quantum_Dom
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Many thanks sonogashira !!! 
Finally I can take a peek at those papers 
Cheers.
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Ephoton
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Mood: trying to figure out why I need a dark room retreat when I live in a forest of wattle.
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do you think this reaction will work for ethylamine.
it states butyl amine as the lowest alphatic amine in it examples.
would nitro ethane azeotrope with the acetone in the dioxane solution.
e3500 console login: root
bash-2.05#
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secunder2
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Can anyone help me if i have a serious problem?
The question is:
that can the phenyl-2-nitrostyrene change to phenyl-2-nitropropene with formaldehyde and if it reacts what kind of catalizator is needed or not needed
to complete the reaction?
thanks everybody
secunder
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Klute
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That's not possible in a one step reaction, and I highly doubt it's possible.
Addition of formaldehyde to the double bond would form 2-nitro-1-phenylpropan-3-ol ("b-(hydromethy)phenyl-b-nitroethane") . You would have to
dehydrate this to obtain the alcene, which would surely partially rearrange to the nitropropene, but both steps would surely give alot of byproducts,
polycondensations and other tar-forming reactions.
\"You can battle with a demon, you can embrace a demon; what the hell can you do with a fucking spiritual computer?\"
-Alice Parr
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secunder2
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First of all thanks again Klute
Then how can I convert my phenyl-2-nitrostyrene to phenyl-2-nitropropene?
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stoichiometric_steve
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| Quote: | Originally posted by secunder2
First of all thanks again Klute
Then how can I convert my phenyl-2-nitrostyrene to phenyl-2-nitropropene? |
yeast
think about other ways to make amphetamine.
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arsenic
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The nitro group in organic synthesis
read the second chapter,
[Edited on by arsenic]
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Filemon
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What does it produce a primary amine with H2O2? a nitroso?
[Edited on 6-8-2008 by Filemon]
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Klute
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An oxide, presumally. hindered secondary amines can form stable nitrosyl radicals (2,2,6,6-tetramethylpiperidine, diisopropylamine, etc..)
\"You can battle with a demon, you can embrace a demon; what the hell can you do with a fucking spiritual computer?\"
-Alice Parr
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Filemon
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Him little that I have found H2O2 it oxidizes a secondary amine to hydroxilamine. It compares the activity of H2O2 with a peracid.
[Edited on 8-8-2008 by Filemon]
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Maja
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What are the conditions when condensing formaldehyde with phenylnitroethane ? For catalyst using some amine or base, but what if formaldehyde is in
water solution 40%? What solvent should I use ?
[Edited on 10-9-2008 by Maja]
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