Oxazole
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| Preferred IUPAC name
1,3-Oxazole[1] | |||
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3D model (JSmol)
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| ECHA InfoCard | 100.005.474 
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| MeSH | D010080 | ||
PubChem CID
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CompTox Dashboard (EPA)
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| Properties | |||
| C3H3NO | |||
| Molar mass | 69.06 g/mol | ||
| Density | 1.050 g/cm3 | ||
| Boiling point | 69 to 70 °C (156 to 158 °F; 342 to 343 K) | ||
| Acidity (pKa) | 0.8 (of conjugate acid) [2] | ||
| Supplementary data page | |||
Structure and
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Refractive index (n), Dielectric constant (εr), etc. | ||
Thermodynamic
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Phase behaviour solid–liquid–gas | ||
Spectral data
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UV, IR, NMR, MS | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |||
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Oxazole is the parent compound for a vast class of heterocyclic aromatic organic compounds. These are azoles with an oxygen and a nitrogen separated by one carbon.[3] Oxazoles are aromatic compounds but less so than the thiazoles. Oxazole is a weak base; its conjugate acid has a pKa of 0.8, compared to 7 for imidazole.
Preparation[]
Classical oxazole synthetic methods in organic chemistry are
- the Robinson–Gabriel synthesis by dehydration of 2-acylaminoketones
- the Fischer oxazole synthesis from cyanohydrins and aldehydes
- the with α-haloketones and formamide
- the Van Leusen reaction with aldehydes and TosMIC
Other methods:
- Oxazolines can also be obtained from cycloisomerization of certain propargyl amides. In one study[4] oxazoles were prepared via a one-pot synthesis consisting of the condensation of and benzoyl chloride to the amide, followed by a Sonogashira coupling of the terminal alkyne end with another equivalent of benzoylchloride, and concluding with p-toluenesulfonic acid catalyzed cycloisomerization:
- In one reported oxazole synthesis the reactants are a nitro-substituted benzoyl chloride and an isonitrile:[5][6]
Biosynthesis[]
In biomolecules, oxazoles result from the cyclization and oxidation of serine or threonine nonribosomal peptides:
Where X = H, CH
3 for serine and threonine respectively, B = base.
(1) Enzymatic cyclization. (2) Elimination. (3) [O] = enzymatic oxidation.
Oxazoles are not as abundant in biomolecules as the related thiazoles with oxygen replaced by a sulfur atom.
Reactions[]
With a pKa of 0.8 for the conjugate acid, oxazoles are far less basic than imidazoles (pKa = 7).[7]
- Deprotonation of oxazoles at C2 is often accompanied by ring-opening to the isonitrile.
- Electrophilic aromatic substitution takes place at C5 requiring activating groups.
- Nucleophilic aromatic substitution takes place with leaving groups at C2.
- Diels–Alder reactions with oxazole dienes can be followed by loss of oxygen to form pyridines.
- The Cornforth rearrangement of 4-acyloxazoles is a thermal rearrangement reaction with the organic acyl residue and the C5 substituent changing positions.
- Various oxidation reactions. One study[8] reports on the oxidation of 4,5-diphenyloxazole with 3 equivalents of CAN to the corresponding imide and benzoic acid:
- In the balanced half-reaction three equivalents of water are consumed for each equivalent of oxazoline, generating 4 protons and 4 electrons (the latter derived from CeIV).
Use of an oxazole in the synthesis of a precursor to pyridoxine, which is converted to vitamin B6.[9]
See also[]
- Isoxazole, an analog with the nitrogen atom in position 2.
- Imidazole, an analog with the oxygen replaced by a nitrogen.
- Thiazole, an analog with the oxygen replaced by a sulfur.
- Benzoxazole, where the oxazole is fused to another aromatic ring.
- Pyrrole, an analog without the oxygen atom.
- Furan, an analog without the nitrogen atom.
- Oxazoline, which has one double bond reduced.
- Oxazolidine, which has both double bonds reduced.
- Oxadiazoles with two nitrogens instead of one (e.g. furazan).
- Oxazolone, an analog with a carbonyl group
References[]
- ^ International Union of Pure and Applied Chemistry (2014). Nomenclature of Organic Chemistry: IUPAC Recommendations and Preferred Names 2013. The Royal Society of Chemistry. p. 140. doi:10.1039/9781849733069. ISBN 978-0-85404-182-4.
- ^ Zoltewicz, J. A. & Deady, L. W. Quaternization of heteroaromatic compounds. Quantitative aspects. Adv. Heterocycl. Chem. 22, 71-121 (1978).
- ^ Heterocyclic Chemistry TL Gilchrist, The Bath press 1985 ISBN 0-582-01421-2
- ^ A new consecutive three-component oxazole synthesis by an amidation–coupling–cycloisomerization (ACCI) sequence Eugen Merkul and Thomas J. J. Müller Chem. Commun., 2006, 4817 - 4819, doi:10.1039/b610839c
- ^ Fully Automated Continuous Flow Synthesis of 4,5-Disubstituted Oxazoles Marcus Baumann, Ian R. Baxendale, Steven V. Ley, Christoper D. Smith, and Geoffrey K. Tranmer Org. Lett.; 2006; 8(23) pp 5231 - 5234; (Letter) doi:10.1021/ol061975c
- ^ They react together in the first phase in a continuous flow reactor to the intermediate enol and then in the second phase in a phosphazene base (PS-BEMP) induced cyclization by solid-phase synthesis.
- ^ Thomas L. Gilchrist "Heterocyclic Chemistry" 3rd ed. Addison Wesley: Essex, England, 1997. 414 pp. ISBN 0-582-27843-0.
- ^ "Ceric Ammonium Nitrate Promoted Oxidation of Oxazoles", David A. Evans, Pavel Nagorny, and Risheng Xu. Org. Lett.; 2006; 8(24) pp 5669 - 5671; (Letter) doi:10.1021/ol0624530
- ^ Gérard Moine, Hans-Peter Hohmann, Roland Kurth, Joachim Paust, Wolfgang Hähnlein, Horst Pauling, Bernd–Jürgen Weimann, Bruno Kaesler (2011). "Vitamins, 6. B Vitamins". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.o27_o09.CS1 maint: uses authors parameter (link)
Categories:
- Oxazoles
- Simple aromatic rings