Anthrone Explained

Anthrone is a tricyclic aromatic ketone. It is used for a common cellulose assay and in the colorimetric determination of carbohydrates.[1]

Derivatives of anthrone are used in pharmacy as laxative. They stimulate the motion of the colon and reduce water reabsorption. Some anthrone derivatives can be extracted from a variety of plants, including Rhamnus frangula, Aloe ferox, Rheum officinale, and Cassia senna. Glycosides of anthrone are also found in high amounts in rhubarb leaves, and alongside concentrated amounts of oxalic acid are the reason for the leaves being inedible.

Synthesis and reactions

Anthrone can be prepared from anthraquinone by reduction with tin or copper.[2]

An alternative synthesis involves cyclization of o-benzylbenzoic acid induced with hydrogen fluoride.[3]

Anthrone condenses with glyoxal to give, following dehydrogenation, acedianthrone, a useful octacyclic pigment.

Tautomer

thumb|center|314px|Tautomeric equilibrium for anthrone.Anthrone is the more stable tautomer relative to the anthrol. The tautomeric equilibrium is estimated at 100 in aqueous solution. For the two other isomeric anthrols, the tautomeric equilibrium is reversed.[4]

Notes and References

  1. Determination of Yeast Carbohydrates with the Anthrone Reagent . Nature . 170 . 626–627 . 1952 . 10.1038/170626a0 . Trevelyan, W. E. . 13002392 . Forrest . RS . Harrison . JS . 4328. 1952Natur.170..626T. 4184596 .
  2. 10.15227/orgsyn.014.0004. Benzanthrone. Organic Syntheses. 1934. 14. 4. L. C.. Macleod. C. F. H.. Allen.
  3. Fieser. Louis F.. Hershberg. E. B.. Inter- and Intramolecular Acylations with Hydrogen Fluoride. Journal of the American Chemical Society. May 1939. 61. 5. 1272–1281. 10.1021/ja01874a079.
  4. 10.1021/jo052615q. 16674042. Tautomeric Equilibria and Pi Electron Delocalization for Some Monohydroxyarenes Quantum Chemical Studies. The Journal of Organic Chemistry. 71. 10. 3727–3736. 2006. Ośmiałowski. Borys. Raczyńska. Ewa D.. Krygowski. Tadeusz M..