Oxazole

The classic synthetic route the Robinson–Gabriel synthesis by dehydration of 2-acylaminoketones:

File:Robinson-Gabriel-Synthese-Übersichtsreaktion.svg

The Fischer oxazole synthesis from cyanohydrins and aldehydes is also widely used:

Image:Fischer_Oxazole_Synthesis.png

Other methods are known including the reaction of α-haloketones and formamide and the Van Leusen reaction with aldehydes and TosMIC.

In biomolecules, oxazoles result from the cyclization and oxidation of serine or threonine nonribosomal peptides:{{cite journal |doi=10.1039/A806930A |title=Thiazole and Oxazole Peptides: Biosynthesis and Molecular Machinery |date=1999 |last1=Roy |first1=Ranabir Sinha |last2=Gehring |first2=Amy M. |last3=Milne |first3=Jill C. |last4=Belshaw |first4=Peter J. |last5=Walsh |first5=Christopher T. |last6=Roy |first6=Ranabir Sinha |last7=Gehring |first7=Amy M. |last8=Milne |first8=Jill C. |last9=Belshaw |first9=Peter J. |last10=Walsh |first10=Christopher T. |journal=Natural Product Reports |volume=16 |issue=2 |pages=249–263 |pmid=10331285 }}

:Image:Biosynthesis of oxazole.png{{clear|left}}

Oxazoles are not as abundant in biomolecules as the related thiazoles with oxygen replaced by a sulfur atom.

With a pK_a of 0.8 for the conjugate acid (oxazolium salts), oxazoles are far less basic than imidazoles (pK_a = 7). Deprotonation of oxazoles occurs at C2, and the lithio salt exists in equilibrium with the ring-opened enolate-isonitrile, which can be trapped by silylation. Formylation with dimethylformamide gives 2-formyloxazole.

Electrophilic aromatic substitution takes place at C5, but requiring electron donating groups.

Nucleophilic aromatic substitution takes place with leaving groups at C2.

Diels–Alder reactions involving oxazole (as dienes) and electrophilic alkenes has been well developed as a route to pyridines. In this way, alkoxy-substituted oxazoles serve a precursors to the pyridoxyl system, as found in vitamin B6. The initial cycloaddition affords a bicyclic intermediate, with an acid-sensitive oxo bridgehead.

File:OxazoleRouteVitaminB6.png, which is converted to vitamin B6.{{cite encyclopedia|title=Vitamins, 6. B Vitamins|encyclopedia=Ullmann's Encyclopedia of Industrial Chemistry|author=Gérard Moine |author2=Hans-Peter Hohmann |author3=Roland Kurth |author4=Joachim Paust |author5=Wolfgang Hähnlein |author6=Horst Pauling |author7=Bernd–Jürgen Weimann |author8=Bruno Kaesler |publisher=Wiley-VCH|place=Weinheim|year=2011|doi=10.1002/14356007.o27_o09|isbn=978-3-527-30673-2 }}]]

In 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"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}} reports on the oxidation of 4,5-diphenyloxazole with 3 equivalents of CAN to the corresponding imide and benzoic acid:

:Image:OxazolineOxidation.png

: 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 Ce^IV).

• Isoxazole, an analog with the nitrogen atom in position 2.
• Thiazole, an analog with the oxygen replaced by a sulfur.
• Benzoxazole, where the oxazole is fused to a benzene ring.
• Oxazoline, which has one double bond reduced.
• Oxazolidine, which has both double bonds reduced.
• Oxazolone, an analog with a carbonyl group

• 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. {{doi|10.1021/ol061975c}}

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Category:Simple aromatic rings