|Primary amine||Secondary amine||Tertiary amine|
Amines are organic compounds and functional groups that contain a basic nitrogen atom with a lone pair. Amines are derivatives of ammonia, where in one or more hydrogen atoms have been replaced by a substituent such as an alkyl or aryl group. Important amines include amino acids, biogenic amines, trimethylamine, and aniline; see Category:Amines for a list of amines. Inorganic derivatives of ammonia are also called amines, such as chloramine (NClH2).
Primary amines misoures arise when one of three hydrogen atoms in the OS ammonia is replaced by an alkyl. Important primary alkyl amines include methylamine, ethanolamine (2-aminoethanol), and the buffering agent tris). Secondary amines have two alkyl substituents bound to N together with one hydrogen. Important representatives include dimethylamine and methylethanolamine. In tertiary amines, all three hydrogen atoms are replaced by organic substituents. Examples include trimethylamine, a distinctively fishy smell. Cyclic amines are either secondary or tertiary amines. Examples of cyclic amines include the 3-member ring aziridine and the six-membered ring piperidine. N-methylpiperidine is a cyclic tertiary amine. It is also possible to have four alkyl substituents on the nitrogen. These compounds are not amines but are called quaternary ammonium cations, have a charged nitrogen center, and necessarily come with an anion.
Aromatic amines have the nitrogen atom connected to an aromatic ring as in anilines. The aromatic ring decreases the alkalinity of the amine, depending on its substituents. The presence of an amine group strongly increases the reactivity of the aromatic ring, due to an electron-donating effect.
Amines are named in several ways. Typically, the compound is given the prefix "amino-" or the suffix: "-amine." The prefix "N-" shows substitution on the nitrogen atom. An organic compound with multiple amino groups is called a diamine, triamine, tetraamine and so forth.
Systematic names for some common amines:
|Lower amines are named with the suffix -amine.
||Higher amines have the prefix amino as a functional group.
Hydrogen bonding significantly influences the properties of primary and secondary amines. Thus the boiling point of amines is higher than those of the corresponding phosphines, but generally lower than those of the corresponding alcohols. Thus methylamine and ethylamine are gases under standard conditions, whereas the corresponding methyl alcohol and ethyl alcohols are liquids. Gaseous amines possess a characteristic ammonia smell, liquid amines have a distinctive "fishy" smell.
Also reflecting their ability to form hydrogen bonds, most aliphatic amines display some solubility in water. Solubility decreases with the increase in the number of carbon atoms. Aliphatic amines display significant solubility in organic solvents, especially polar organic solvents. Primary amines react with ketones such as acetone, and most amines are incompatible with chloroform and carbon tetrachloride.
The aromatic amines, such as aniline, have their lone pair electrons conjugated into the benzene ring, thus their tendency to engage in hydrogen bonding is diminished. Their boiling points are high and their solubility in water low
Amines of the type NHRR' and NRR'R" are chiral: the nitrogen atom bears four substituents counting the lone pair. The energy barrier for the inversion of the stereocenter is relatively low, e.g., ~7 kcal/mol for a trialkylamine. The interconversion of the stereoisomers has been compared to the inversion of an open umbrella in to a strong wind. Because of this low barrier, amines such as NHRR' cannot be resolved optically and NRR'R" can only be resolved when the R, R', and R" groups are constrained in cyclic structures such as aziridines. Quaternary ammonium salts with four distinct groups on the nitrogen are capable of exhibiting optical activity.
The nitrogen atom features a lone electron pair that can bind H+ to form an ammonium ion R3NH+. The lone electron pair is represented in this article by a two dots above or next to the N. The water solubility of simple amines is largely due to hydrogen bonding between protons on the water molecules and these lone electron pairs.
|Ions of compound||Kb|
|Ammonia NH3||1.8·10−5 M|
|Propylamine CH3CH2CH2NH2||4.7·10−4 M|
|2-Propylamine (CH3)2CHNH2||3.4·10−4 M|
|Methylamine CH3NH2||4.4·10−4 M|
|Dimethylamine (CH3)2NH||5.4·10−4 M|
|Trimethylamine (CH3)3N||5.9·10−5 M|
|Ions of compound||Kb|
|Ammonia NH3||1.8·10−5 M|
|Aniline C6H5NH2||3.8·10−10 M|
|4-Methylaniline 4-CH3C6H4NH2||1.2·10−9 M|
|Ions of compound||Maximum number of H-bond|
|NH4+||4 Very Soluble in H2O|
|R3NH+||1 Least Soluble in H2O|
In sterically hindered amines, as in the case of trimethylamine, the protonated form is not well-solvated. For this reason the parent amine is less basic than expected. In the case of aprotic polar solvents (like DMSO and DMF), wherein the extent of solvation is not as high as in protic polar solvents (like water and methanol), the basicity of amines is almost solely governed by the electronic factors within the molecule.
The most industrially significant amines are prepared from ammonia by alkylation in amine alkylation. Haloalkanes react with amines to give a corresponding alkyl-substituted amine, with the release of a halogen acid. Such reactions, which are most useful for alkyl iodides and bromides, are rarely employed because the degree of alkylation is difficult to control.
Nitriles are reduced to amines using hydrogen in the presence of a nickel catalyst, although acidic or alkaline conditions should be avoided to avoid hydrolysis of -CN group. LiAlH4 is more commonly employed for the reduction of nitriles on the laboratory scale. Similarly, LiAlH4 reduces amides to amines.
Aniline and its derivatives are prepared by reduction of the nitroaromatics. Many laboratory methods exist for the preparation of amines, many of these methods being rather specialized.
|Gabriel synthesis||organohalide||reagent: potassium phthalimide|
|Staudinger reduction||Azide||This reaction also takes place with a reducing agent such as lithium aluminium hydride.|
|Schmidt reaction||carboxylic acid|
|Aza-Baylis-Hillman reaction||imine||Synthesis of allylic amines|
|Hofmann degradation||amide||This reaction is valid for preparation of primary amines only. Gives good yields of primary amines uncontaminated with other amines.|
|Hofmann Elimination||Quaternary ammonium salt||upon treatment with strong base|
|Reduction of nitro compounds||nitro compounds||can be accomplished with elemental zinc, tin or iron with an acid.|
|Delepine reaction||organohalide||reagent hexamine|
|Buchwald-Hartwig reaction||aryl halide||specific for aryl amines|
|Menshutkin reaction||tertiary amine||reaction product a quaternary ammonium cation|
|hydroamination||alkenes and alkynes|
The dominant reactivity of amines is their nucleophilicity. Most primary amines are good ligands for metal ions to give coordination complexes. Amines are alkylated by alkyl halides. Acyl chlorides and acid anhydrides react with primary and secondary amines to form amides (the "Schotten-Baumann reaction").
Because amines are basic, they neutralize acids to form the corresponding ammonium salts R3NH+. When formed from carboxylic acids and primary and secondary amines, these salts thermally dehydrate to form the corresponding amides.
Amines react with nitrous acid to give diazonium salts. The alkyl diazonium salts spontaneously decompose by losing N2 to produce a mixture of alkenes, alkanols or alkyl halides, with alkanols as the major product. This reaction is of little synthetic importance because the diazonium salt formed is too unstable.
Primary aromatic amines, such as aniline ("phenylamine") form more stable diazonium salts, which can be isolated in the crystalline form. These species undergo a variety of synthetically useful transformations. With cuprous cyanide the corresponding nitrile is formed. Arenediazonium ions undergo coupling with electron-rich aromatic compounds such as a phenol to form an azo compound. These species are widely used as dyes.
Reduction of the imines gives secondary amines:
Similarly, secondary amines react with ketones and aldehydes to form enamines:
An amine reaction overview is given below:
|Reaction name||Reaction product||Comment|
|Amine alkylation||amines||degree of substitution increases|
|Schotten-Baumann reaction||amides||Reagents: acyl chlorides, acid anhydrides|
|Hinsberg reaction||sulfonamides||Reagents: sulfonyl chlorides|
|Organic oxidation||nitroso compounds||Reagent: peroxymonosulfuric acid|
|Organic oxidation||diazonium salt||Reagent: nitrous acid|
|Zincke reaction||Zincke aldehyde||reagent pyridinium salts , with primary and secondary amines|
|Emde degradation||tertiary amine||reduction of quaternary ammonium cations|
|Hofmann-Martius rearrangement||aryl substituted anilines|
|Von Braun reaction||Organocyanamide||By cleavage (tertiary amines only) with cyanogen bromide|
Many kinds of biological activity produce amines by breakdown of amino acids. Many natural neurotransmitters like epinephrine, norepinephrine, dopamine, serotonine, histamine are amines.
Primary aromatic amines are used as a starting material for the manufacture of azo dyes. It reacts with nitric(III) acid to form diazonium salt, which can undergo coupling reaction to form azo compound. As azo-compounds are highly coloured, they are widely used in dyeing industries, such as:
Many drugs are designed to mimic or to interfere with the action of natural amine neurotransmitters, exemplified by the amine drugs:
Low molecular weight amines are toxic and some are easily absorbed through the skin. Many higher molecular weight amines are highly active biologically.