Pyridine
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| Pyridine | |
|---|---|
 |
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| IUPAC name | Pyridine |
| Other names | Azabenzene Azine py |
| Identifiers | |
| CAS number | [110-86-1] |
| SMILES | C1=NC=CC=C1 |
| Properties | |
| Molecular formula | C5H5N |
| Molar mass | 79.101 g/mol |
| Appearance | colourless liquid |
| Density | 0.9819 g/cm³, liquid |
| Melting point |
−41.6 °C |
| Boiling point |
115.2 °C |
| Solubility in water | Miscible |
| Viscosity | 0.94 cP at 20 °C |
| Hazards | |
| MSDS | External MSDS |
| EU classification | Flammable (F) Harmful (Xn) |
| NFPA 704 |
 3
2
0
|
| R-phrases | R20 R21 R22 R34 R36 R38 |
| Flash point | 21 °C |
| Related compounds | |
| Related amines | Picoline Quinoline |
| Related compounds | Aniline Pyrimidine Piperidine |
| Supplementary data page | |
| Structure and properties |
n, εr, etc. |
| Thermodynamic data |
Phase behaviour Solid, liquid, gas |
| Spectral data | UV, IR, NMR, MS |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox disclaimer and references |
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Pyridine is a chemical compound with the formula C5H5N. It is a liquid with a distinctively putrid, fishy 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".
Contents |
[edit] 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[1] because protonation does not disrupt the aromatic pi system.
[edit] 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.
[edit] 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.[2] 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.
[edit] 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:[3] 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.[4]
- 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[5]
- 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) [6] a malonate ester salt reacts with dichloromethylamine [7]
[edit] 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.[8] [9]
[edit] 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".[10] 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.[10] Effects of an acute pyridine intoxication include dizziness, headache, nausea and anorexia. Further symptoms include abdominal pain and pulmonary congestion.[10] Although resistant to oxidation, pyridine is readily degraded by bacteria to ammonium and carbon dioxide.[11]
[edit] 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.
[edit] 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
- 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 Pyramidine
- 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.
[edit] See also
- Simple aromatic rings
- 6-Membered aromatic rings with one carbon replaced by another group: borabenzene, silabenzene, germanabenzene, stannabenzene, phosphorine, pyrylium salt
[edit] References
- ^ T. M. Krygowski, H. Szatyowicz, and J. E. Zachara J. Org. Chem. 2005 70(22) 8859 - 8865; doi:10.1021/jo051354h.
- ^ Sherman, A. R. “Pyridine” in e-EROS (Encyclopedia of Reagents for Organic Synthesis) (Ed: L. Paquette) 2004, J. Wiley & Sons, New York. doi:10.1002/047084289X.rp280 Article Online Posting Date: April 15, 2001.
- ^ Gilchrist, T.L. (1997). Heterocyclic Chemistry ISBN 0470204818
- ^ Shinkichi Shimizu, Nanao Watanabe, Toshiaki Kataoka, Takayuki Shoji, Nobuyuki Abe, Sinji Morishita, Hisao Ichimura "Pyridine and Pyridine Derivatives" in "Ullmann's Encyclopedia of Industrial Chemistry" 2007; John Wiley & Sons: New York.
- ^ Ciamician-Dennstedt Rearrangement @ drugfuture.com Link
- ^ Eine Synthese von Pyridin-Derivaten Berichte der deutschen chemischen Gesellschaft Volume 49, Issue 1, Date: Januar-Juni 1916, Pages: 494-501 L. Gattermann, A. Skita doi:10.1002/cber.19160490155
- ^ Gattermann-Skita @ Institute of Chemistry, Skopje, Macedonia http://www.pmf.ukim.edu.mk/PMF/Chemistry/reactions/gattermann-skita.htm
- ^ Histamine Antagonists. Basically Substituted Pyridine Derivatives Charles H. Tilford, Robert S. Shelton, and M. G. van Campen J. Am. Chem. Soc.; 1948; 70(12) pp 4001 - 4009; doi:10.1021/ja01192a010
- ^ Eine Synthese von -Pyridyl-dialkyl-carbinolen Bruno Emmert, Erich Asendorf Berichte der deutschen chemischen Gesellschaft; 1939; 72(6) pp 1188 - 1194; doi:10.1002/cber.19390720610
- ^ a b c International Agency for Research on Cancer (IARC) (2000-08-22). Pyridine Summary & Evaluation (HTML). IARC Summaries & Evaluations. IPCS INCHEM. Retrieved on 2007-01-17.
- ^ Sims, G.K. and O'Loughlin, E.J. (1989). "Degradation of pyridines in the environment". CRC Critical Reviews in Environmental Control 19 (4): 309-340.
[edit] External links
- International Chemical Safety Card 0323
- NIOSH Pocket Guide to Chemical Hazards
- Computational Chemistry Wikif Pyridines]
- Synthesis of pyridines (overview of recent methods)
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