Robinson–Gabriel synthesis
The Robinson–Gabriel synthesis is a chemical reaction that forms substituated oxazoles by dehydration of 2-acylamino-ketones. [1] [2][3] It is named after Sir Robert Robinson and Siegmund Garbriel who described the reaction
2-Acylamino-ketones can be synthesized using the Dakin–West reaction.
Reaction Mechanism
The first part of this reaction is the cyclization of an 2-acylamidoketone that contains all three oxazole substituents. The second part is a dehydration, removing water from the molecule [4]. Labeling studies have determined that the amide oxygen is the most Lewis basic and therefore is the one included in the oxazole [5].
Modifications
Cyclodehydrating Agents
Many cyclodehydrating agents have been discovered to be of use in the Robinson-Gabriel synthesis. Historically, the dehydration agent is concentrated sulfuric acid. To date, the reaction has been shown to proceed with a variety of other agents including phosphorous pentachloride, phosphorous pentoxide, phosphoryl chloride, thyonyl chloride, phosphoric acid-acetic anhydride, polyphosphoric acid, and anhydrous hydrogen fluoride [6]
Applications
References
- ^ Robinson, R. J. Chem. Soc. 1909, 95, 2167.
- ^ Gabriel, S. Ber. 1910, 43, 134.
- ^ Gabriel, S. Ber. 1910, 43, 1283.
- ^ Turchi, I. (Sept 15, 2009). Heterocyclic Chemistry in Drug Discovery. John Wiley & Sons. p. 235. ISBN 978-1-118-14890-7.
{{cite book}}: Check date values in:|date=(help) - ^ Wasserman, H. J. Org. Chem 1973, 38, 2407-2408.
- ^ Turchi, I. (Sept 15, 2009). The Chemistry of Heterocyclic Compounds, Oxazoles. John Wiley & Sons. p. 3. ISBN 9780471869580.
{{cite book}}: Check date values in:|date=(help)
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