Tetrahydropyran

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This article is about tetrahydropyran, whose IUPAC name is oxane. For ethylene oxide, which has occasionally been named as oxane, see oxirane.
Tetrahydropyran
Tetrahydropyran
THP
Names
Preferred IUPAC name
Oxane
Other names
Tetrahydropyran,
Oxacyclohexane,
1,5-epoxypentane
Identifiers
  • 142-68-7 checkY
3D model (JSmol)
102436
ChEBI
ChemSpider
DrugBank
ECHA InfoCard 100.005.048 Edit this at Wikidata
EC Number
  • 205-552-8
UNII
Properties
C5H10O
Molar mass 86.134 g·mol−1
Density 0.880 g/cm3
Melting point −45 °C (−49 °F; 228 K)
Boiling point 88 °C (190 °F; 361 K)
Hazards
Main hazards Flammable, Causes skin irritation
NFPA 704 (fire diamond)
2
4
1
Flash point −15.6 °C (3.9 °F; 257.5 K)
Lethal dose or concentration (LD, LC):
LDLo (lowest published)
 3000 mg/kg (oral, rat)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY  (what is checkY☒N ?)
Infobox references

Tetrahydropyran (THP) is the organic compound consisting of a saturated six-membered ring containing five carbon atoms and one oxygen atom. It is named by reference to pyran, which contains two double bonds, and may be produced from it by adding four hydrogens. In 2013, its preferred IUPAC name was established as oxane.[1] The compound is a colourless volatile liquid. Derivatives of tetrahydropyran are, however, more common. 2-Tetrahydropyranyl (THP-) ethers derived from the reaction of alcohols and 3,4-dihydropyran are commonly used as protecting groups in organic synthesis.[2] Furthermore, a tetrahydropyran ring system, i.e., five carbon atoms and an oxygen, is the core of pyranose sugars, such as glucose.

Structure and preparation[]

In gas phase, the THP exists in its lowest energy Cs symmetry chair conformation.[3]

One classic procedure for the organic synthesis of tetrahydropyran is by hydrogenation of the 3,4-isomer of dihydropyran with Raney nickel.[4]

Tetrahydropyranyl derivatives[]

Although tetrahydropyran is an obscure compound, tetrahydropyranyl ethers are commonly used in organic synthesis. Specifically, the 2-tetrahydropyranyl (THP) group is a common protecting group for alcohols.[5][6] Alcohols react with 3,4-dihydropyran to give 2-tetrahydropyranyl ethers. These ethers are resilient to a variety of reactions. The alcohol can later be restored by acid-catalyzed hydrolysis. This hydrolysis reforms the parent alcohol as well as 5-hydroxypentanal. THP ethers derived from chiral alcohols form diastereomers. Another undesirable feature is that the ethers display complex NMR spectra, which interfere with analysis.[2]

Protection of alcohol as THP ether followed by deprotection. Both steps require acid catalysts.

In a typical procedure, the alcohol is treated with 3,4-dihydropyran and p-toluenesulfonic acid in dichloromethane at ambient temperature.[2]

THP protection used in the total synthesis of solandelactone E[7]

Alternatively, the THP ether can be generated under the conditions akin to those for the Mitsunobu reaction. Thus the alcohol is treated with 2-hydroxytetrahydropyranyl, triphenylphosphine, and diethyl azodicarboxylate (DEAD) in tetrahydrofuran (THF).

Commonly, THP ethers are deprotected using acetic acid in a THF/water solution, p-toluenesulfonic acid in water, or Pyridinium p-toluenesulfonate (PPTS) in ethanol.

Oxanes[]

Oxanes are the class of hexic cyclic ether rings with tetrahydropyran as the root chemical. Oxanes have one or more carbon atoms replaced with an oxygen atom.[8] The IUPAC preferred name for tetrahydropyran is now oxane.[9]

See also[]

  • Pyran
  • Dioxane and Trioxane, which have two and three oxygen atoms as part of their six-membered rings respectively

References[]

  1. ^ "New IUPAC Organic Nomenclature - Chemical Information BULLETIN" (PDF).
  2. ^ Jump up to: a b c Wuts, Peter G. M.; Greene, Theodora W. (2006). "Protection for the Hydroxyl Group, Including 1,2‐ and 1,3‐Diols". Greene's Protective Groups in Organic Synthesis (4th ed.). pp. 16–366. doi:10.1002/9780470053485.ch2. ISBN 9780470053485.
  3. ^ Builth-Williams, J. D.; Bellm, S. M.; Chiari, L.; Thorn, P. A.; Jones, D. B.; Chaluvadi, H.; Madison, D. H.; Ning, C. G.; Lohmann, B. (2013). "A dynamical (e,2e) investigation of the structurally related cyclic ethers tetrahydrofuran, tetrahydropyran, and 1,4-dioxane" (PDF). Journal of Chemical Physics. 139 (3): 034306. doi:10.1063/1.4813237. hdl:2328/26887.
  4. ^ Andrus, D. W.; Johnson, John R. (1943). "Tetrahydropyran". Organic Syntheses. 23: 90. doi:10.15227/orgsyn.023.0090.; Collective Volume, 3, p. 794
  5. ^ Earl, R. A.; Townsend, L. B. (1981). "Methyl 4-Hydroxy-2-butynoate". Organic Syntheses. 60: 81. doi:10.15227/orgsyn.060.0081.; Collective Volume, 7, p. 334
  6. ^ Kluge, Arthur F. (1986). "Diethyl [(2-Tetrahydropyranyloxy)methyl]phosphonate". Organic Syntheses. 64: 80. doi:10.15227/orgsyn.064.0080.; Collective Volume, 7, p. 160
  7. ^ Robinson, Anna; Aggarwal, Varinder K. (2010). "Asymmetric Total Synthesis of Solandelactone E: Stereocontrolled Synthesis of the 2-ene-1,4-diol Core through a Lithiation–Borylation–Allylation Sequence". Angewandte Chemie International Edition. 49 (37): 6673–6675. doi:10.1002/anie.201003236.
  8. ^ Ferenc Notheisz, Mihály Bartók, "Hydrogenolysis of C–O, C–N and C–X bonds", p. 416 in, R. A. Sheldon, Herman van Bekkum (eds), Fine Chemicals through Heterogeneous Catalysis, John Wiley & Sons, 2008 ISBN 3527612971.
  9. ^ "New IUPAC Organic Nomenclature - Chemical Information BULLETIN" (PDF).
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