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. 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.
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 Bredereck reaction 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 oxazoles were prepared via a one-pot synthesis consisting of the condensation of propargyl amine 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:
In biomolecules, oxazoles result from the cyclization and oxidation of serine or threonine nonribosomal peptides:
Oxazoles are not as abundant in biomolecules as the related thiazoles with oxygen replaced by a sulfur atom.
With a pKa of 0.8 for the conjugate acid, oxazoles are far less basic than imidazoles (pKa = 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.
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Electrophilic aromatic substitution is an organic reaction in which an atom that is attached to an aromatic system (usually hydrogen) is replaced by an electrophile. Some of the most important electrophilic aromatic substitutions are aromatic nitration, aromatic halogenation, aromatic sulfonation, and alkylation and acylation Friedel–Crafts reaction. The most widely practised example of this reaction is the ethylation of benzene. Approximately 24,700,000 tons were produced in 1999.
Imidazole (ImH) is an organic compound with the formula C3N2H4. It is a white or colourless solid that is soluble in water, producing a mildly alkaline solution. In chemistry, it is an aromatic heterocycle, classified as a diazole, and has non-adjacent nitrogen atoms in meta-substitution. Many natural products, especially alkaloids, contain the imidazole ring. These imidazoles share the 1,3-C3N2 ring but feature varied substituents. This ring system is present in important biological building blocks, such as histidine and the related hormone histamine.
Furan is a heterocyclic organic compound, consisting of a five-membered aromatic ring with four carbon atoms and one oxygen atom. Chemical compounds containing such rings are also referred to as furans. Furan is a colorless, flammable, highly volatile liquid with a boiling point close to room temperature. It is soluble in common organic solvents, including alcohol, ether, and acetone, and is slightly soluble in water. Its odor is "strong, ethereal; chloroform-like". It is toxic and may be carcinogenic in humans.
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