Orcinol

Synthesis and reactions

Orcinol was first prepared by dehydroacetic acid, a conversion that involved ring-opening of the pyrone to a triketone. This early experiment helped establish the rich condensation chemistry of polyketides.{{cite journal|title=Polyketide Biosynthesis: A Millennium Review It can be obtained by fusing extract of aloes with potash, followed by acidification.

It undergoes O-methylation with dimethylsulfate.

It is used in the production of the dye orcein and as a reagent in some chemical tests for pentoses, such as Bial's Test. It may be synthesized from toluene; more interesting is its production when acetone dicarboxylic ester is condensed with the aid of sodium. It crystallizes in colorless prisms with one molecule of water, which redden on exposure to air. Ferric chloride gives a bluish-violet coloration with the aqueous solution. Unlike resorcinol it does not give a fluorescein with phthalic anhydride. Oxidation of the ammoniacal solution gives orcein, C28H24N2O7, the chief constituent of the natural dye archil. 4-Methylcatechol is an isomer, found as its methyl ether (creosol) in beech-wood tar.

:[[File:Orcin Merck 820933.jpg|thumb|none|]]

Production from shale oil

Orcinol is also found in shale oil produced from Kukersite oil shale. It is the main water-soluble phenol in the oil, and has been extracted and refined industrially by Viru Keemia Grupp.

References

References

1. ''[[Merck Index]]'', 11th Edition, '''6819'''.
2. Robiquet: „Essai analytique des lichens de l'orseille", ''[[Annales de chimie et de physique]]'', '''1829''', ''42'', p. 236–257.
3. R. N. Mirrington. (1973). "Orcinol Monomethyl Ether". Org. Synth..
4. {{EB1911
5. (2020-10-28). "Vapor Pressures of Phenolic Compounds Found in Pyrolysis Oil". Journal of Chemical & Engineering Data.
6. "Fine chemicals".