Piperidine

Piperidine[1]
Names
Preferred IUPAC name
Piperidine[2]
Other names
Hexahydropyridine
Azacyclohexane
Pentamethyleneamine
Azinane
Identifiers
110-89-4 YesY
3D model (Jmol) Interactive image
ChEBI CHEBI:18049 YesY
ChEMBL ChEMBL15487 YesY
ChemSpider 7791 YesY
ECHA InfoCard 100.003.467
5477
PubChem 8082
RTECS number TM3500000
UNII 67I85E138Y YesY
Properties
C5H11N
Molar mass 85.15 g·mol−1
Appearance colourless liquid
Density 0.862 g/mL, liquid
Melting point −7 °C (19 °F; 266 K)
Boiling point 106 °C (223 °F; 379 K)
miscible
Acidity (pKa) 11.22[3]
Viscosity 1.573 cP at 25 °C
Hazards
Safety data sheet MSDS1,MSDS2
Flammable (F)
Toxic (T)
R-phrases R11, R23/24, R34
NFPA 704
Flammability code 3: Liquids and solids that can be ignited under almost all ambient temperature conditions. Flash point between 23 and 38 °C (73 and 100 °F). E.g., gasoline) Health code 3: Short exposure could cause serious temporary or residual injury. E.g., chlorine gas Reactivity code 3: Capable of detonation or explosive decomposition but requires a strong initiating source, must be heated under confinement before initiation, reacts explosively with water, or will detonate if severely shocked. E.g., fluorine Special hazards (white): no codeNFPA 704 four-colored diamond
3
3
3
Related compounds
Related compounds
 pyridine
pyrrolidine
piperazine
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Piperidine is an organic compound with the molecular formula (CH2)5NH. This heterocyclic amine consists of a six-membered ring containing five methylene bridges (–CH2–) and one amine bridge (–NH–). It is a colorless liquid with an odor described as objectionable, and typical of amines. [4] the name comes from the genus name Piper, which is the Latin word for pepper.[5] Although, piperidine is a common organic compound, it is best known as a representative structure element within many pharmaceuticals and alkaloids.

Production

Piperidine was first reported in 1850 by the Scottish chemist Thomas Anderson and again, independently, in 1852 by the French chemist Auguste Cahours, who named it.[6][7][8] Both men obtained piperidine by reacting piperine with nitric acid.

Industrially, piperidine is produced by the hydrogenation of pyridine, usually over a molybdenum disulfide catalyst:[9]

C5H5N + 3 H2 → C5H10NH

Pyridine can also be reduced to piperidine via a modified Birch reduction using sodium in ethanol.[10]

Natural occurrence of piperidine and derivatives

Piperidine itself has been obtained from black pepper,[11][12] from Psilocaulon absimile (Aizoaceae),[13] and in Petrosimonia monandra.[14]

The piperidine structural motif is present in numerous natural alkaloids. These include piperine, which gives black pepper its spicy taste. This gave the compound its name. Other examples are the fire ant toxin solenopsin,[15] the nicotine analog anabasine of tree tobacco (Nicotiana glauca), lobeline of Indian tobacco, and the toxic alkaloid coniine from poison hemlock, which was used to put Socrates to death.[16]

Conformation

Piperidine prefers a chair conformation, similar to cyclohexane. Unlike cyclohexane, piperidine has two distinguishable chair conformations: one with the N–H bond in an axial position, and the other in an equatorial position. After much controversy during the 1950s–1970s, the equatorial conformation was found to be more stable by 0.72 kcal/mol in the gas phase.[17] In nonpolar solvents, a range between 0.2 and 0.6 kcal/mol has been estimated, but in polar solvents the axial conformer may be more stable.[18] The two conformers interconvert rapidly through nitrogen inversion; the free energy activation barrier for this process, estimated at 6.1 kcal/mol, is substantially lower than the 10.4 kcal/mol for ring inversion.[19] In the case of N-methylpiperidine, the equatorial conformation is preferred by 3.16 kcal/mol,[17] which is much larger than the preference in methylcyclohexane, 1.74 kcal/mol.

axial conformation
equatorial conformation

Reactions

Piperidine is a widely used secondary amine. It is widely used to convert ketones to enamines.[20] Enamines derived from piperidine can be used in the Stork enamine alkylation reaction.[21]

Piperidine can be converted to the chloramine C5H10NCl with calcium hypochlorite. The resulting chloramine undergoes dehydrohalogenation to afford the cyclic imine.[22]

NMR chemical shifts

Uses

Piperidine is used as a solvent and as a base. The same is true for certain derivatives: N-formylpiperidine is a polar aprotic solvent with better hydrocarbon solubility than other amide solvents, and 2,2,6,6-tetramethylpiperidine is a highly sterically hindered base, useful because of its low nucleophilicity and high solubility in organic solvents.

A significant industrial application of piperidine is for the production of dipiperidinyl dithiuram tetrasulfide, which is used as a rubber vulcanization accelerator.[9]

List of piperidine medications

Minoxidil is a piperidine derivative widely used to prevent hair loss.

Piperidine and its derivatives are ubiquitous building blocks in the synthesis of pharmaceuticals and fine chemicals. The piperidine structure is found in, for example:

Piperidine is also commonly used in chemical degradation reactions, such as the sequencing of DNA in the cleavage of particular modified nucleotides. Piperidine is also commonly used as a base for the deprotection of Fmoc-amino acids used in solid-phase peptide synthesis.

Piperidine is listed as a Table II precursor under the United Nations Convention Against Illicit Traffic in Narcotic Drugs and Psychotropic Substances due to its use (peaking in the 1970s) in the clandestine manufacture of PCP (1-(1-phenylcyclohexyl)piperidine, also known as angel dust, sherms, wet, etc.).[23]

References

  1. ↑ International Chemical Safety Card 0317
  2. ↑ Nomenclature of Organic Chemistry : IUPAC Recommendations and Preferred Names 2013 (Blue Book). Cambridge: The Royal Society of Chemistry. 2014. p. 142. doi:10.1039/9781849733069-FP001. ISBN 978-0-85404-182-4.
  3. ↑ Hall, H. K. (1957). "Correlation of the Base Strengths of Amines". J. Am. Chem. Soc. 79: 5441–5444. doi:10.1021/ja01577a030.
  4. ↑ Frank Johnson Welcher (1947). Organic Analytical Reagents. D. Van Nostrand. p. 149.
  5. ↑ Senning, Alexander (2006). Elsevier's Dictionary of Chemoetymology. Amsterdam: Elsevier. ISBN 0-444-52239-5.
  6. ↑ Warnhoff, Edgar W. (1998). "When piperidine was a structural problem" (PDF). Bulletin of the History of Chemistry. 22: 29–34.
  7. ↑ Anderson, Thomas (1850). "Vorläufiger Bericht über die Wirkung der Salpetersäure auf organische Alkalien" [Preliminary report on the effect of nitric acid on organic alkalis]. Annalen der Chemie und Pharmacie. 75: 80–83. doi:10.1002/jlac.18500750110.
  8. ↑ Cahours, Auguste (1852). "Recherches sur un nouvel alcali dérivé de la pipérine" [Investigations of a new alkali derived from piperine]. Comptes rendus. 34: 481–484. L'alcali nouveau dérivé de la pipérine, que je désignerai sous le nom de 'pipéridine',… (The new alkali derived from piperine, which I will designate by the name of 'piperidine',…
  9. 1 2 Eller, Karsten; Henkes, Erhard; Rossbacher, Roland; Höke, Hartmut (2005), "Amines, aliphatic", Ullmann's Encyclopedia of Industrial Chemistry, Weinheim: Wiley-VCH, doi:10.1002/14356007.a02_001
  10. ↑ Marvel, C. S.; Lazier, W. A. (1941). "Benzoyl Piperidine". Org. Synth.; Coll. Vol., 1, p. 99
  11. ↑ Späth; Englaender (1935). "Über das Vorkommen von Piperidin im schwarzen Pfeffer". Chemische Berichte. 68: 2218–2221. doi:10.1002/cber.19350681211.
  12. ↑ Pictet, Amé; Pictet, René (1927). "Sur l'alcaloïde volatil du poivre". Helvetica Chimica Acta. 10: 593–595. doi:10.1002/hlca.19270100175.
  13. ↑ Rimington, Claude (1934). "Psilocaulon absimile N.E.Br. as a stock poison". South African Journal of Science. 31: 184–193.
  14. ↑ Juraschewski; Stepanov (1939). J. Gen. Chem. USSR. 9: 1687. Missing or empty |title= (help)
  15. ↑ Arbiser, J. L.; Kau, T.; Konar, M.; et al. (2007). "Solenopsin, the alkaloidal component of the fire ant (Solenopsis invicta), is a naturally occurring inhibitor of phosphatidylinositol-3-kinase signaling and angiogenesis". Blood. 109 (2): 560–5. doi:10.1182/blood-2006-06-029934. PMC 1785094Freely accessible. PMID 16990598.
  16. ↑ Thomas Anderson Henry (1949). The Plant Alkaloids (4th ed.). The Blakiston Company.
  17. 1 2 Carballeira, Luis; Pérez Juste, Ignacio (1998). "Influence of calculation level and effect of methylation on axial/equatorial equilibria in piperidines". Journal of Computational Chemistry. 19 (8): 961–976. doi:10.1002/(SICI)1096-987X(199806)19:8<961::AID-JCC14>3.0.CO;2-A.
  18. ↑ Blackburne, Ian D.; Katritzky, Alan R.; Yoshito Takeuchi (1975). "Conformation of piperidine and of derivatives with additional ring hetero atoms". Acc. Chem. Res. 8 (9): 300–306. doi:10.1021/ar50093a003.
  19. ↑ Anet, F. A. L.; Yavari, Issa (1977). "Nitrogen inversion in piperidine". J. Am. Chem. Soc. 99 (8): 2794–2796. doi:10.1021/ja00450a064.
  20. ↑ Kane, Vinayak V.; Jones, Maitland, Jr. (1990). "Spiro[5.7]trideca-1,4-dien-3-one". Org. Synth.; Coll. Vol., 7, p. 473
  21. ↑ Smith, Michael B.; March, Jerry (2001). March's Advanced Organic Chemistry: Reactions, Mechanisms, and Structure (5th ed.). Wiley-Interscience. ISBN 0-471-58589-0.
  22. ↑ Claxton, George P.; Allen, Lloyd; Grisar, J. Martin (1988). "2,3,4,5-Tetrahydropyridine trimer". Org. Synth.; Coll. Vol., 6, p. 968
  23. ↑ "List of Precursors and Chemicals Frequently Used in the Illicit Manufacture of Narcotic Drugs and Psychotropic Substances Under International Control" (PDF). International Narcotics Control Board. Archived from the original (PDF) on 2008-02-27.
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