Phenols

In organic chemistry, phenols, sometimes called phenolics, are a class of chemical compounds consisting of one or more hydroxyl groups (−OH) bonded directly to an aromatic hydrocarbon group.^[1] The simplest is phenol, C₆H₅OH. Phenolic compounds are classified as simple phenols or polyphenols based on the number of phenol units in the molecule.

Phenols are both synthesized industrially and produced by plants and microorganisms.^[2]

Phenols are more acidic than typical alcohols. The acidity of the hydroxyl group in phenols is commonly intermediate between that of aliphatic alcohols and carboxylic acids (their pK_a is usually between 10 and 12). Deprotonation of a phenol forms a corresponding negative phenolate ion or phenoxide ion, and the corresponding salts are called phenolates or phenoxides (aryloxides according to the IUPAC Gold Book).

Phenols are susceptible to Electrophilic aromatic substitutions. Condensation with formaldehyde gives resinous materials, famously Bakelite.

Another industrial-scale electrophilic aromatic substitution is the production of bisphenol A, which is produced by the condensation with acetone.^[3]

Phenol is readily alkylated at the ortho positions using alkenes in the presence of a Lewis acid such as aluminium phenoxide:

CH₂=CR₂ + C₆H₅OH → R₂CHCH₂-2-C₆H₄OH

More than 100,000 tons of tert-butyl phenols are produced annually (year: 2000) in this way, using isobutylene (CH₂=CMe₂) as the alkylating agent. Especially important is 2,6-ditert-butylphenol, a versatile antioxidant.^[3]

Phenols undergo esterification. Phenol esters are active esters, being prone to hydrolysis. Phenols are reactive species toward oxidation. Oxidative cleavage, for instance cleavage of 1,2-dihydroxybenzene to the monomethylester of 2,4 hexadienedioic acid with oxygen, copper chloride in pyridine^[4] Oxidative de-aromatization to quinones also known as the Teuber reaction.^[5] and oxone.^[6] In reaction depicted below 3,4,5-trimethylphenol reacts with singlet oxygen generated from oxone/sodium carbonate in an acetonitrile/water mixture to a para-peroxyquinole. This hydroperoxide is reduced to the quinole with sodium thiosulfate.

Phenols are oxidized to hydroquinones in the Elbs persulfate oxidation.

Reaction of naphtols and hydrazines and sodium bisulfite in the Bucherer carbazole synthesis.

Many phenols of commercial interest are prepared by elaboration of phenol or cresols. They are typically produced by the alkylation of benzene/toluene with propylene to form cumene then O₂ is added with H₂SO₄ to form phenol (Hock process). In addition to the reactions above, many other more specialized reactions produce phenols:

• rearrangement of esters in the Fries rearrangement^[7][8]
• rearrangement of N-phenylhydroxylamines in the Bamberger rearrangement^[9][10]
• dealkylation of phenolic ethers
• reduction of quinones
• replacement of an aromatic amine by an hydroxyl group with water and sodium bisulfide in the Bucherer reaction^[11]
• thermal decomposition of aryl diazonium salts, the salts are converted to phenol^[12]
• by the oxidation of aryl silanes—an aromatic variation of the Fleming-Tamao oxidation^[13]
• catalytic synthesis from aryl bromides and iodides using nitrous oxide^[14]

There are various classification schemes.^[15]:2 A commonly used scheme is based on the number of carbons and was devised by Jeffrey Harborne and Simmonds in 1964 and published in 1980:^[15]:2[16]

More than 371 drugs approved by the FDA between the years of 1951 and 2020 contain either a phenol or a phenolic ether (a phenol with an alkyl), with nearly every class of small molecule drugs being represented, and natural products making up a large portion of this list.^[17]

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