Phenolates
Salts or other derivatives of phenols
Phenolates (also called phenoxides) are anions, salts, and esters of phenols, containing the phenolate ion. They may be formed by reaction of phenols with strong base.
01Properties
Alkali metal phenolates, such as sodium phenolate hydrolyze in aqueous solution to form basic solutions. At pH = 10, phenol and phenolate are in approximately 1:1 proportions.
The phenoxide anion (aka phenolate) is a strong nucleophile with a comparable to the one of carbanions or tertiary amines. Generally, oxygen attack of phenoxide anions is kinetically favored, while carbon-attack is thermodynamically preferred (see Thermodynamic versus kinetic reaction control). Mixed oxygen/carbon attack and by this a loss of selectivity is usually observed if the reaction rate reaches diffusion control.
02Uses
Alkyl aryl ethers can be synthesized through the Williamson ether synthesis by treating sodium phenolate with an alkyl halide:
- C6H5ONa + CH3I → C6H5OCH3 + NaI
- C6H5ONa + (CH3O)2SO2 → C6H5OCH3 + (CH3O)SO3Na
Production of salicylic acid
Salicylic acid is produced in the Kolbe-Schmitt reaction between carbon dioxide and sodium phenolate.
Sources and credits
This article is adapted from the Wikipedia article “Phenolates”, written by its contributors and licensed under CC BY-SA 4.0. Fathomly has changed the layout, removed citation markers, navigation and maintenance notices, and adjusted punctuation. This adapted version is shared under the same license. For references, see the original article.
Images, from Wikimedia Commons:
- Phenolate.svg by Leyo, Public domain
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