Originally posted by Madandcrazy
Surely a couple of amines can oxidized when it is the correct
oxidizer/solvent to the reaction and the amin component is not decomposed or is stable for this.
I belive any different methods existing, when a amin should oxidized i a aromatic ring with H2SO4/H2O2, it is certainly more easy as when a azin component should oxidized.
What should you do when for instance the reaction with the glycin and the chloroamin should oxidized to the follow ?
COOH-CH2-NH2
-->
COOH-CH2-NHNH2
-->
COOH-CH2-NHNO2
It would possibly give not the desired end-product, but it would give maybe glycin anhydride.
Intersted is maybe when chloromethane should treated with
ammonium acetate and dilute HCl to aminomethane, is it not eventually the endproduct Cl-CH2-NH2 ?
Should this way walk too when some components was easyer threated with bromin, maybe
the glycin anhydride should brominated to
dibromoglycin anhydride -->
diaminoglycin anhydride -->
2,5-dinitrogylcin anhydride |