Phenyl salicylate

Phenyl salicylate, or salol, is the organic compound with the formula C₆H₅O₂C₆H₄OH. It is a white solid. It is occasionally used in sunscreens and as an antiseptic.

Production and reactions

The title compound was synthesized first in 1883 by the Polish chemist and doctor Marceli Nencki (who didn't publish his findings) and then independently in 1885 by the German chemist Richard Seifert ( de) (1861–1919) (who did publish his findings). It is synthesized by heating salicylic acid with phenol in the presence of phosphoryl chloride. It also arises from heating salicylic acid:
:2HOC₆H₄CO₂H → C₆H₅O₂C₆H₄OH + CO₂ + H₂O
The conversion entails dehydration and decarboxylation. Heating phenyl salicylate in turn gives xanthone.
:2C₆H₅O₂C₆H₄OH → 2C₆H₅OH + O ₆H₄sub>2CO + CO₂
In this conversion, phenol is produced as well as carbon dioxide.

Salol reaction

In the salol reaction, phenyl salicylate reacts with ''o''-toluidine in 1,2,4-trichlorobenzene at elevated temperatures to the corresponding amide ''o''-salicylotoluide. Salicylamides are a type of drug.

Medical

It has been used as an antiseptic based on the antibacterial activity upon hydrolysis in the small intestine.

It acts as a mild analgesic.

History

The Swiss physician Hermann Sahli (sometimes spelled "Saly") (1856–1933) sought a substitute for sodium salicylate, which was used as a treatment for rheumatoid arthritis but which wasn't tolerated by some patients. So Dr. Sahli asked the Polish chemist and doctor Marceli Nencki of Bern, Switzerland, if he knew of a salicylate compound that lacked sodium salicylate's side effects. Nencki recommended phenyl salicylate, which he had synthesized circa 1883. While Nencki had been investigating how phenyl salicylate behaved in the body, he hadn't published his findings. Meanwhile, the German chemist Richard Seifert ( de) (1861–1919), a student of the German chemist Rudolf Wilhelm Schmitt ( de) (1830–1898), independently synthesized phenyl salicylate in 1885. In 1885, Seifert accepted a position at the Heyden chemical corporation ( de) of Radebeul, Germany, which manufactured salicylic acid. The United States granted to Nencki and Seifert a patent for the production of phenyl salicylate,Nencki, Marrel V. ; Seifert, Richar
"Production of salol"
U.S. Patent no. 350,012 (filed: 22 July 1886 ; issued: 28 September 1886). whereas Germany granted a patent for its production to Nencki and the Heyden corporation. The Heyden company subsequently sold phenyl salicylate as a pharmaceutical, under the commercial name "Salol", a contraction of "SALicylate of phenOL". Among other applications, Salol was used as an orally administered antiseptic for the small intestine, where the compound is hydrolyzed into salicylic acid and phenol.

See also

Phenyl salicylate is used in school laboratory demonstrations on how cooling rates affect crystal size in igneous rocks, and can be used to demonstrate seed crystal selectiveness.

References

{{Urologicals, including antispasmodics

Phenol esters
Salicylate esters
1886 introductions
3-Hydroxypropenals