pyridine or azine, C₅H₅N, colorless, flammable, toxic liquid with a putrid odor. It melts at -42°C; and boils at 115.5°C;. Chemically, it is a heterocyclic aromatic tertiary amine (see under amino group). Its molecule resembles that of benzene, one carbon-hydrogen unit in the benzene ring being replaced with a nitrogen molecule. It is miscible with water and with most organic solvents. Its aqueous solution is slightly alkaline. Pyridine is used as a solvent, as a denaturant for alcohol, and as a starting material in the synthesis of other compounds. Compounds that can be derived from pyridine include antihistamines and vitamins. Pyridine is obtained from bone oil or from coal tar by destructive distillation, which decomposes alkaloids that contain it. Alkaloids that contain pyridine include coniine, piperine (the alkaloid in pepper), and nicotine (present in tobacco); free pyridine is present in tobacco smoke.

Any of a class of aromatic compounds with a six-member aromatic ring composed of five carbon atoms and one nitrogen atom, making it a heterocyclic compound. The simplest one is pyridine itself (C₅H₅N). Natural compounds with pyridine rings include niacin and pyridoxine (see vitamin B complex), the tuberculosis drug isoniazid, and several plant products (e.g., nicotine). Pyridine is used as a raw material for various drugs, vitamins, and fungicides and as a solvent. Because it has a nauseating odour and a burning taste, it is added to ethanol and antifreezes to make them undrinkable (see denaturation).

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| Section8 = }} Pyridine is a chemical compound with the formula C₅H₅N. It is a liquid with a distinctively putrid, fish-like odour. Pyridine is a simple and fundamentally important heterocyclic aromatic organic compound. It is structurally related to benzene, wherein one CH group in the six-membered ring is replaced by a nitrogen atom. The pyridine ring occurs in many important compounds, including the nicotinamides. Pyridine is sometimes used as a ligand in coordination chemistry. As a ligand, it is usually abbreviated "py".

Basicity

The nitrogen atom on pyridine features a basic lone pair of electrons. Because this lone pair is not delocalized into the aromatic pi-system, pyridine is basic with chemical properties similar to tertiary amines. The pKa of the conjugate acid is 5.21. Pyridine is protonated by reaction with acids and forms a positively charged aromatic polyatomic ion called pyridinium cation. The bond lengths and bond angles in pyridine and the pyridinium ion are almost identical because protonation does not disrupt the aromatic pi system. In addition, the pyridinium cation is isoelectronic with benzene.

Pyridine as a solvent

Pyridine is a widely used and versatile solvent: it is polar but aprotic. It is miscible with a broad range of solvents including hexane and water. Deuterated pyridine, called pyridine-d₅, is a common solvent for¹H NMR spectroscopy.

Role in chemical synthesis

Pyridine is important in industrial chemistry, both as a fundamental building block and as a solvent and reagent in organic synthesis. It is used as a solvent in Knoevenagel condensations.

It is also a starting material in the synthesis of compounds used as an intermediate in making insecticides, herbicides, pharmaceuticals, food flavorings, dyes, rubber chemicals, adhesives, paints, explosives and disinfectants. Pyridine is also used as a denaturant for antifreeze mixtures, for ethyl alcohol, for fungicides, and as a dyeing aid for textiles.

Role in chemical analysis

Pyridine, along with barbituric acid, is commonly used in colorimetric determinations of cyanide in aqueous matrices. Pyridine reacts with cyanogen chloride (formed in an earlier step by reaction of the cyanide anion with chloramine-T) to form a conjugated species that couples two molecules of barbituric acid together, forming a red-colored dye. Color intensity is directly proportional to cyanide concentration.

Pyridine was originally used as the base in the Karl Fischer titration, but has since been largely replaced by imidazole, which is more basic than pyridine, allowing for a more stable equivalence point and a faster reaction rate. Imidazole also has the advantage of being odorless.

Preparation and occurrence

Many methods exist in industry and in the laboratory (some of them named reactions) for the synthesis of pyridine and its derivatives: Pyridine was originally isolated industrially from crude coal tar. It is currently synthesized from acetaldehyde, formaldehyde and ammonia, a process that involves the intermediacy of acrolein:

CH₂O + NH₃ + 2 CH₃CHO → C₅H₅N + 3 H₂O

By substituting other aldehydes for acetaldehyde, one obtains alkyl and aryl substituted pyridines. 26,000 tons were produced worldwide in 1989.

• The Hantzsch pyridine synthesis is a multicomponent reaction involving formaldehyde, a keto-ester and a nitrogen donor.
• Other examples of the pyridine class can be formed by the reaction of 1,5-diketones with ammonium acetate in acetic acid followed by oxidation. This reaction is called the Kröhnke pyridine synthesis.
• Pyridinium salts can be obtained in the Zincke reaction.
• The Ciamician-Dennstedt Rearrangement (1881) is the ring-expansion of pyrrole with dichlorocarbene to 3-chloropyridine and HCl
• In the Chichibabin pyridine synthesis (Aleksei Chichibabin, 1906) the reactants are three equivalents of a linear aldehyde and ammonia
• In the Gattermann-Skita synthesis (1916) a malonate ester salt reacts with dichloromethylamine

Organic reactions

In organic reactions pyridine behaves both as a tertiary amine, undergoing protonation, alkylation, acylation, and N-oxidation at nitrogen, and as an aromatic compound, undergoing Nucleophilic substitutions.

• Pyridine is a good nucleophile with a donor number of 33.1. It is easily attacked by alkylating agents to give N-alkylpyridinium salts.
• Nucleophilic aromatic substitution occurs at C2/C4. For example in the Chichibabin reaction, pyridine reacts with sodium amide to give 2-aminopyridine. In the Emmert reaction (Bruno Emmert, 1939) pyridine reacts with a ketone in presence of aluminium or magnesium and mercuric chloride to give the carbinol also at C2.

Safety and environmental

The LD₅₀ in rats (oral) is 891 mg kg^–1. It is volatile and can be absorbed through skin. Available data indicate that "exposure to pyridine in drinking-water led to reduction of sperm motility at all dose levels in mice and increased estrous cycle length at the highest dose level in rats". Currently its evaluations as a possible carcinogenic agent showed there is inadequate evidence in humans for the carcinogenicity of pyridine, albeit there is limited evidence of carcinogenic effects on animals. Effects of an acute pyridine intoxication include dizziness, headache, nausea and anorexia. Further symptoms include abdominal pain and pulmonary congestion. Although resistant to oxidation, pyridine is readily degraded by bacteria to ammonia and carbon dioxide.

Derivatives

• Pyridine-borane, C₅H₅NBH₃ (m.p. 10–11 °C) is a mild reducing agent with improved stability relative to NaBH₄ in protic solvents and improved solubility in aprotic organic solvents.
• Pyridine-sulfur trioxide, C₅H₅NSO₃ (mp 175 °C) is a sulfonation agent used to convert alcohols to sulfonates, which in turn undergo C-O bond scission upon reduction with hydride agents
• Cetylpyridinium chloride is a cationic surfactant and a widely used disinfection and antiseptic agent.

Related compounds

Structurally or chemically related compounds are

• DMAP is short for 4-dimethylaminopyridine
• Bipyridine and viologen are simple polypyridine compounds consisting of two pyridine molecules joined by a single bond
• The herbicides paraquat and diquat are quarterny N-alkylammonium salts of 4,4'- and 2,2'-bipyridine
• Terpyridine, a molecule of three pyridine rings connected together by two single bonds.
• Quinoline and Isoquinoline have pyridine and a benzene ring fused together.
• Aniline is a benzene derivative with an attached NH₂ group and NOT a pyridine
• Diazines are compounds with one more carbon replaced by nitrogen such as Pyrazine and Pyrimidine
• Triazines are compounds with two more carbons replaced by nitrogen and a tetrazine has four nitrogen atoms
• 2,6-Lutidine is a trivial name for 2,6-dimethylpyridine.
• Collidine is the trivial name for 2,4,6-trimethylpyridine.
• Pyridinium p-toluenesulfonate (PPTS) is a salt formed by proton exchange between pyridine and p-toluenesulfonic acid
• 2-Chloropyridine is a toxic environmentally significant component of the breakdown of the pesticide imidacloprid.

See also

• Simple aromatic rings
• 6-Membered aromatic rings with one carbon replaced by another group: borabenzene, silabenzene, germanabenzene, stannabenzene, phosphorine, pyrylium salt

References

External links

• International Chemical Safety Card 0323
• NIOSH Pocket Guide to Chemical Hazards
• Synthesis of pyridines (overview of recent methods)