Guaiacol

Guaiacol (/ˈɡwaɪəkɒl/) is a naturally-occurring organic compound with the formula C6H4(OH)(OCH3). Although it is biosynthesized by a variety of organisms,[3] this aromatic oil is usually derived from guaiacum or wood creosote. It is also found in essential oils from celery seeds, tobacco leaves, orange leaves, and lemon peels.[4] It is colorless but samples become yellow upon exposure to air and light. Guaiacol is present in wood smoke, resulting from the pyrolysis of lignin. The compound contributes to the flavor of many substances such as whisky[5] and roasted coffee.[6]

Guaiacol[1]
Names
IUPAC name
2-Methoxyphenol
Other names
o-Methoxyphenol
O-Methylcatechol[2]
2-Hydroxyanisole
Pyroguaiac acid
Pyrocatechol monomethyl ether
1-hydroxy-2-methoxybenzene
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.001.786
KEGG
UNII
Properties
C7H8O2
Molar mass 124.139 g·mol−1
Appearance colorless oil or crystalline solid
Density 1.112 g/cm3, liquid
1.129 g/cm3, crystals
Melting point 26–29 °C (79–84 °F; 299–302 K)
Boiling point 204–206 °C (399–403 °F; 477–479 K)
23.3 g/l at 25 °C
Related compounds
Mequinol
3-Methoxyphenol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Preparation

The compound was first isolated by Otto Unverdorben in 1826.[7] Guaiacol is produced by methylation of o-catechol, for example using potash and dimethyl sulfate:[8]

C6H4(OH)2 + (CH3O)2SO2 → C6H4(OH)(OCH3) + HO(CH3O)SO2

Laboratory methods

Guaiacol can be prepared by diverse routes in the laboratory. o-Anisidine, derived in two steps from anisole, can be hydrolyzed via its diazonium derivative. Guaiacol can be synthesized by the dimethylation of catechol followed by selective mono-demethylation.[9]

C6H4(OCH3)2 + C2H5SNa[10] → C6H4(OCH3)(ONa) + C2H5SCH3

Uses and chemical reactions

Guaiacol is useful precursor for the synthesis of other compounds.[11] Being derived from biomass, it is a potential component or precursor to "green fuels".[12]

Medicinal and food

Guaiacol is a precursor to various flavorants, such as eugenol.[13] An estimated 85% of the world's supply of vanillin comes from guaiacol. The route entails condensation of glyoxylic acid with guaiacol to give mandelic acid, which is oxidized to produce a phenylglyoxylic acid. This acid undergoes a decarboxylation to afford vanillin.[14]

Guaiacol is also used medicinally as an expectorant, antiseptic, and local anesthetic.[15]

Guaiacol is produced in the gut of desert locusts, Schistocerca gregaria, by the breakdown of plant material. This process is undertaken by the gut bacterium Pantoea agglomerans (Enterobacter). It is one of the main components of the pheromones that cause locust swarming.[16]

Safety

Methoxyphenols are potential biomarkers of biomass smoke exposure, such as from inhalation of woodsmoke. Dietary sources of methoxyphenols overwhelm the contribution from inhalational exposures to woodsmoke.[17]

See also

References
  1. Merck Index (13th ed.). p. 4568.
  2. "List of synonyms for guaiacol". Chemindustry.
  3. Duffey, S. S.; Aldrich, J. R.; Blum, M. S. (1977). "Biosynthesis of phenol and guaiacol by the hemipteran Leptoglossus phyllopus". Comparative Biochemistry and Physiology B: Biochemistry & Molecular Biology. 56 (2B): 101–102. doi:10.1016/0305-0491(77)90029-3. PMID 830476.
  4. Burdock, G. A. (1995). Encyclopedia of Food and Color Additives. Boca Raton, FL: CRC Press. p. 1244–1245. ISBN 978-0849394126.
  5. Gallegos, Jenna (August 17, 2017). "The best way to drink whiskey, according to science". The Washington Post. Guaiacol is what gives whiskey that smoky, spicy, peaty flavor.
  6. Dorfner, R.; Ferge, T.; Kettrup, A.; Zimmermann, R.; Yeretzian, C. (Sep 2003). "Real-time monitoring of 4-vinylguaiacol, guaiacol, and phenol during coffee roasting by resonant laser ionization time-of-flight mass spectrometry". Journal of Agricultural and Food Chemistry. 51 (19): 5768–5773. doi:10.1021/jf0341767. ISSN 0021-8561. PMID 12952431.
  7. Stevens, M. E.; Ronan, A. K.; Sourkes, T. S.; E. M., Boyd (1943). "On the Expectorant Action of Creosote and the Guaiacols". Canadian Medical Association Journal. 48 (2): 124–127. PMC 1827660. PMID 20322688.
  8. Fiege, Helmut; Voges, Heinz-Werner; Hamamoto, Toshikazu; Umemura, Sumio; Iwata, Tadao; Miki, Hisaya; Fujita, Yasuhiro; Buysch, Hans-Josef; Garbe. "Phenol Derivatives". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a19_313.
  9. Mirrington, R. N.; Feutrill, G. I. (1988). "Orcinol Monomethyl Ether". Organic Syntheses.; Collective Volume, 6, p. 859
  10. Sodium ethanethiolate
  11. Liao, Chun-Chen (2005). "Masked o-benzoquinone strategy in organic synthesis: Short and efficient construction of cis-decalins and linear triquinanes from 2-methoxyphenols". Pure and Applied Chemistry. 77 (7): 1221–1234. doi:10.1351/pac200577071221.
  12. Saidi, Majid; Samimi, Fereshteh; Karimipourfard, Dornaz; Nimmanwudipong, Tarit; Gates, Bruce C.; Rahimpour, Mohammad Reza (2014). "Upgrading of lignin-derived bio-oils by catalytic hydrodeoxygenation". Energy Environ. Sci. 7: 103–129. doi:10.1039/C3EE43081B.
  13. Allen, C. F. H.; Gates, J. W., Jr (1955). "o-Eugenol". Organic Syntheses.; Collective Volume, 3, p. 418
  14. Esposito, Lawrence J.; Formanek, K.; Kientz, G.; Mauger, F.; Maureaux, V.; Robert, G.; Truchet, F. (1997). "Vanillin". Kirk–Othmer Encyclopedia of Chemical Technology. 24 (4th ed.). New York, NY: John Wiley & Sons. pp. 812–825.
  15. "Guaiacol". DrugBank. 2019-11-02. Retrieved 2019-11-18.
  16. Dillon, Rod J.; Vennard, Chris T.; Charnley, A. Keith (2000-02-24). "Pheromones: Exploitation of gut bacteria in the locust". Nature. 403 (6772): 851. Bibcode:2000Natur.403..851D. doi:10.1038/35002669. PMID 10706273.
  17. Smith, K. R. (2005). "Critical review of the health effects of woodsmoke" (PDF). School of Public Health, University of Berkeley. Archived from the original (PDF) on 2009-07-10.
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