Chemistry:3,4-Dihydropyran
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| Names | |
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| Preferred IUPAC name
3,4-Dihydro-2H-pyran | |
| Other names
2,3-Dihydro-4H-pyran, DHP
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| Identifiers | |
3D model (JSmol)
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| ChEMBL | |
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PubChem CID
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| UNII | |
| UN number | 2376 |
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| Properties | |
| C5H8O | |
| Molar mass | 84.118 g·mol−1 |
| Appearance | Colorless liquid |
| Density | 0.922 g/mL |
| Melting point | −70 °C (−94 °F; 203 K) |
| Boiling point | 86 °C (187 °F; 359 K) |
| Hazards | |
| GHS pictograms |  
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| GHS Signal word | Danger |
| H225, H315, H317, H319 | |
| P210, P233, P240, P241, P242, P243, P261, P264, P272, P280, P302+352, P303+361+353, P305+351+338, P321, P332+313, P333+313, P337+313, P362, P363, P370+378, P403+235, P501 | |
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 | |
3,4-Dihydropyran (DHP) is a heterocyclic compound with the formula C5H8O. The six-membered C5O ring has the unsaturation adjacent to oxygen. The isomeric 3,6-dihydropyran has a methylene separating the double bond and oxygen. DHP is used for protecting group for alcohols. It is a colorless liquid.[1]
Preparation
Dihydropyran is prepared by the dehydration of tetrahydrofurfuryl alcohol over alumina at 300–400 °C.[2] THFA is itself prepared from tetrahydro-2-furoic acid.
Reactions
In organic synthesis, the 2-tetrahydropyranyl (THP) group is used as a protecting group for alcohols.[3][4] Reaction of the alcohol with DHP forms a THP ether, protecting the alcohol from a variety of reactions. The alcohol can later be restored by acidic hydrolysis, concomitant with formation of 5-hydroxypentanal.[5]
See also
- Pyran
- Tetrahydropyran
References
- ↑ Paul Ch. Kierkus (2001). "3,4-Dihydro-2H-pyran". EEROS. doi:10.1002/047084289X.rd230. ISBN 0471936235.
- ↑ R. L. Sawyer and D. W. Andrus (1955). "2,3-Dihydropyran". Organic Syntheses. http://www.orgsyn.org/demo.aspx?prep=cv3p0276.; Collective Volume, 3, pp. 276
- ↑ R. A. Earl L. B. Townsend (1990). "Methyl 4-Hydroxy-2-butynoate". Organic Syntheses. http://www.orgsyn.org/demo.aspx?prep=cv7p0334.; Collective Volume, 7, pp. 334
- ↑ Arthur F. Kluge (1990). "Diethyl [(2-Tetrahydropyranyloxy)methyl]phosphonate". Organic Syntheses. http://www.orgsyn.org/demo.aspx?prep=cv7p0160.; Collective Volume, 7, pp. 160
- ↑ 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.
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