Eucaine
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| Trade names | Beta-Eucaine |
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| Formula | C15H21NO2 |
| Molar mass | 247.338 g·mol−1 |
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Eucaine, also known as β-eucaine or Betacaine, is a drug that was previously used as a local anesthetic.[1] It was designed as an analog of cocaine and was one of the first synthetic chemical compounds to find general use as an anesthetic.[2] It is a white, crystalline solid. Prior to World War I, Britain imported eucaine from Germany.[3] During the war, a team including Jocelyn Field Thorpe and Martha Annie Whiteley developed a synthesis in Britain.[3]
The brand name Betacaine can sometimes refer to a preparation containing lidocaine, not eucaine.
Synthesis
[edit]_synthesis.svg)
Condensation of diacetonamine [625-04-7] (1) with acetaldehyde (paraldehyde) rather than acetone gives the piperidone containing one less methyl group, i.e. 2,2,6-trimethylpiperidin-4-one [3311-23-7] (2). Reduction of the ketone with sodium amalgam gives the alcohol as a mixture of isomers, 2,2,6-trimethylpiperidin-4-ol (3). Benzoylation then affords beta-eucaine (4).
See also
[edit]- α-Eucaine, a related local anesthetic
References
[edit]- ^ Sneader W (31 October 2005). Drug Discovery: A History. John Wiley & Sons. pp. 127–9. ISBN 978-0-470-01552-0.
- ^ Manske RH (12 May 2014). The Alkaloids: Chemistry and Physiology. Elsevier. pp. 213–4. ISBN 978-1-4832-2192-2.
- ^ a b Creese MR (1997). "Martha Annie Whiteley (1866-1956): Chemist and Editor" (PDF). Bulletin for the History of Chemistry. 8: 42–45.
- ^ Organic medical chemicals, by M. Barrowliff, 98-99, 1921.
- ^ Harries, C. (1918). "Untersuchungen über die cyclischen Acetonbasen". Justus Liebig's Annalen der Chemie 417 (2-3): 107–191. doi:10.1002/jlac.19184170202.
- ^ King, Harold (1924). "VII.—Stereoisomerism and local anœsthetic action in the β-eucaine group. Resolution of β- and iso-β-eucaine". J. Chem. Soc., Trans. 125 (0): 41–57. doi:10.1039/CT9242500041.
External links
[edit]
The dictionary definition of eucaine at Wiktionary
