Phenols

In organic chemistry, phenols, sometimes called phenolics, are a class of chemical compounds consisting of one or more hydroxyl groups (—O H) bonded directly to an aromatic hydrocarbon group. The simplest is phenol, C
₆H
₅OH. Phenolic compounds are classified as simple phenols or polyphenols based on the number of phenol units in the molecule.

Phenol – the simplest of the phenols.

Chemical structure of salicylic acid, the active metabolite of aspirin.

Phenols are both synthesized industrially and produced by plants and microorganisms.[1]

Properties

Acidity

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).

Condensation with aldehydes and ketones

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.[2]

C-Alkylation with alkenes

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.[2]

Other reactions

Phenols undergo esterfication. 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[3] Oxidative de-aromatization to quinones also known as the Teuber reaction.[4] and oxone.[5] 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

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 O
₂ is added with H
₂SO
₄ to form phenol (Hock process). In addition to the reactions above, many other more specialized reactions produce phenols:

rearrangement of esters the Fries rearrangement
rearrangement of N-phenylhydroxylamines in the Bamberger rearrangement
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
thermal decomposition of aryl diazonium salts, the salts are converted to phenol[6]
by the oxidation of aryl silanes—an aromatic variation of the Fleming-Tamao oxidation [7]

Classification

The best-selling drug in the U.S. is Acetaminophen, also known as Paracetamol is a phenol.

There are various classification schemes.[8]^: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:[8]^:2[9]

Phenol	the parent compound, used as a disinfectant and for chemical synthesis
Bisphenol A	and other bisphenols produced from ketones and phenol / cresol
BHT	(butylated hydroxytoluene) - a fat-soluble antioxidant and food additive
4-Nonylphenol	a breakdown product of detergents and nonoxynol-9
Orthophenyl phenol	a fungicide used for waxing citrus fruits
Picric acid	(trinitrophenol) - an explosive material
Phenolphthalein	pH indicator
Xylenol	used in antiseptics & disinfectants

Drugs and bioactive natural products

tyrosine	one of the 20 standard amino acids
L-DOPA	dopamine prodrug used to treat Parkinson's disease
propofol	short-acting intravenous anesthetic agent
vitamin K hydroquinone	blood-clotting agent that converts
levothyroxine (L-thyroxine)	Top-selling drug to treat thyroid hormone deficiency.
amoxicillin	Top-selling antibiotic
estradiol	the major female sex hormone

gollark: BORING! I have a better idea.

gollark: I suppose I could probably come up with something where it would *cause* a kernel panic if run as root.

gollark: I couldn't find more convincing kernel panic messages.

gollark: ```cvoid* malloc(size_t n) { printf("Kernel panic. Shutting down."); exit(-3)}```

gollark: Then we need it.

References

Hättenschwiler, Stephan; Vitousek, Peter M. (2000). "The role of polyphenols in terrestrial ecosystem nutrient cycling". Trends in Ecology & Evolution. 15 (6): 238–243. doi:10.1016/S0169-5347(00)01861-9. PMID 10802549.
Fiege H; Voges H-W; Hamamoto T; Umemura S; Iwata T; Miki H; Fujita Y; Buysch H-J; Garbe D (2000). "Phenol Derivatives". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a19_313.
2,4-Hexadienedioic acid, monomethyl ester, (Z,Z)- Organic Syntheses, Coll. Vol. 8, p.490 (1993); Vol. 66, p.180 (1988) Article
"2,5-Cyclohexadiene-1,4-dione, 2,3,5-trimethyl". Organic Syntheses. 52: 83. 1972.
Carreño, M. Carmen; González-López, Marcos; Urbano, Antonio (2006). "Oxidative De-aromatization of para-Alkyl Phenols into para-Peroxyquinols and para-Quinols Mediated by Oxone as a Source of Singlet Oxygen". Angewandte Chemie International Edition. 45 (17): 2737–2741. doi:10.1002/anie.200504605. PMID 16548026.
H. E. Ungnade, E. F. Orwoll (1943). "3-Bromo-4-hydroxytoluene". Organic Syntheses. 23: 11. doi:10.15227/orgsyn.023.0011.
Bracegirdle, Sonia; Anderson, Edward A. (2010). "Arylsilane oxidation—new routes to hydroxylated aromatics". Chem. Comm. 46 (20): 3454–6. doi:10.1039/b924135c. PMID 20582346.
Wilfred Vermerris and Ralph Nicholson. Phenolic Compound Biochemistry Springer, 2008
Harborne, J. B. (1980). "Plant phenolics". In Bell, E. A.; Charlwood, B. V. (eds.). Encyclopedia of Plant Physiology, volume 8 Secondary Plant Products. Berlin Heidelberg New York: Springer-Verlag. pp. 329–395.

This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.

[Hattenschwiler-1] Hättenschwiler, Stephan; Vitousek, Peter M. (2000). "The role of polyphenols in terrestrial ecosystem nutrient cycling". Trends in Ecology & Evolution. 15 (6): 238–243. doi:10.1016/S0169-5347(00)01861-9. PMID 10802549.

[Fiege-2] Fiege H; Voges H-W; Hamamoto T; Umemura S; Iwata T; Miki H; Fujita Y; Buysch H-J; Garbe D (2000). "Phenol Derivatives". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a19_313.

[3] 2,4-Hexadienedioic acid, monomethyl ester, (Z,Z)- Organic Syntheses, Coll. Vol. 8, p.490 (1993); Vol. 66, p.180 (1988) Article

[4] "2,5-Cyclohexadiene-1,4-dione, 2,3,5-trimethyl". Organic Syntheses. 52: 83. 1972.

[5] Carreño, M. Carmen; González-López, Marcos; Urbano, Antonio (2006). "Oxidative De-aromatization of para-Alkyl Phenols into para-Peroxyquinols and para-Quinols Mediated by Oxone as a Source of Singlet Oxygen". Angewandte Chemie International Edition. 45 (17): 2737–2741. doi:10.1002/anie.200504605. PMID 16548026.

[6] H. E. Ungnade, E. F. Orwoll (1943). "3-Bromo-4-hydroxytoluene". Organic Syntheses. 23: 11. doi:10.15227/orgsyn.023.0011.

[7] Bracegirdle, Sonia; Anderson, Edward A. (2010). "Arylsilane oxidation—new routes to hydroxylated aromatics". Chem. Comm. 46 (20): 3454–6. doi:10.1039/b924135c. PMID 20582346.

[Vermerris-8] Wilfred Vermerris and Ralph Nicholson. Phenolic Compound Biochemistry Springer, 2008

[Harborne-9] Harborne, J. B. (1980). "Plant phenolics". In Bell, E. A.; Charlwood, B. V. (eds.). Encyclopedia of Plant Physiology, volume 8 Secondary Plant Products. Berlin Heidelberg New York: Springer-Verlag. pp. 329–395.