Amine oxide
From Wikipedia, the free encyclopedia
An amine oxide, also known as amine-N-oxide and N-oxide, is a chemical compound that contains the functional group R3N+-O− (sometimes written as R3N=O or R3N→O). In the strict sense the term amine oxide applies only to oxides of tertiary amines including nitrogen-containing aromatic compounds like pyridine, but is sometimes also used for the analogous derivatives of primary and secondary amines.
Amine oxides are used as protecting group for amines and as chemical intermediates. Long-chain alkyl amine oxides are used as nonionic surfactants and foam stabilizers.
Amine oxide are highly polar molecules have a high polarity close to that of quaternary ammonium salts. Small amine oxides are very hydrophilic and have an excellent water solubility and a very poor solubility in most organic solvents.
Amine oxides are weak bases with a pKa of around 4.5 that form R3N+-OH, cationic hydroxylamines, upon protonation at a pH below their pKa.
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[edit] Synthesis
Amine oxides are prepared by oxidation of tertiary amines or pyridine analogs with hydrogen peroxide (H2O2) or peracids like mCPBA in N-oxidation.
[edit] Reactions
[edit] Pyrolytic elimination
Amine oxides, when heated to 150 to 200 ºC eliminate a hydroxylamine, resulting in an alkene. This pyrolytic syn-elimination reaction is known under the name Cope reaction. The mechanism is similar to that of the Hofmann elimination.
[edit] Reduction to amines
Amine oxides are readily converted to the parent amine by common reduction reagents including lithium aluminum hydride, sodium borohydride, catalytic reduction, zinc / acetic acid, and iron / acetic acid.
[edit] Metabolites
Amine oxides are common metabolites of medication and psychoactive drugs. Examples include nicotine, Zolmitriptan, and morphine.
[edit] Prodrugs
Amine oxides of anti-cancer drugs have been developed as prodrugs that are metabolized in the oxygen deficient cancer tissue to the active drug.
[edit] See also
- Functional group
- Amine, NR3
- Hydroxylamine, NR2OH
- Sulfoxide, R2S=O
- Azoxy, RN=N+(O–)R RN=N+RO−
- N-Methylmorpholine N-oxide, an amine oxide
- TEMPO (2,2,6,6-Tetramethylpiperidine-1-oxyl), a stable amine oxide radical
