2,4,6-Tri-tert-butylphenol
Names
Preferred IUPAC name
2,4,6-Tri-tert-butylphenol
Other names
2,4,6-TTBP
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard 100.010.900
EC Number
  • 211-989-5
UNII
  • InChI=1S/C18H30O/c1-16(2,3)12-10-13(17(4,5)6)15(19)14(11-12)18(7,8)9/h10-11,19H,1-9H3
    Key: PFEFOYRSMXVNEL-UHFFFAOYSA-N
  • CC(C)(C)C1=CC(=C(C(=C1)C(C)(C)C)O)C(C)(C)C
Properties
C18H30O
Molar mass 262.437 g·mol−1
Hazards
GHS labelling:
GHS07: Exclamation markGHS09: Environmental hazard
Warning
H302, H315, H319, H410
P264, P270, P273, P280, P301+P312, P302+P352, P305+P351+P338, P321, P330, P332+P313, P337+P313, P362, P391, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

2,4,6-Tri-tert-butylphenol (2,4,6-TTBP) is a phenol symmetrically substituted with three tert-butyl groups and thus strongly sterically hindered. 2,4,6-TTBP is a readily oxidizable aromatic compound and a weak acid. It oxidizes to give the deep-blue 2,4,6-tri-tert-butylphenoxy radical.[1] 2,4,6-TTBP is related to 2,6-di-tert-butylphenol, which is widely used as an antioxidant in industrial applications. These compounds are colorless solids.[2]

Preparation

The preparation of 2,4,6-tri-tert-butylphenol has been studied extensively. As early as 1890, Wilhelm Koenigs described the acid-catalyzed reaction of phenol with isobutylene.[3] Many other reports have appeared.[4] Yields up to 90% have been reported. Typical side products are the result of incomplete alkylation: 4-tert-butylphenol (4-TBP), 2,4-di-tert-butylphenol (2,4-DTBP), 2,6-di-tert-butylphenol (2,6-DTBP). 2,5-Di-tert-butylphenol (2,5-DTB) has been observed.[5] 2,4,6-tri-tert-butylphenol is also found as a by-product in the synthesis of the disubstitution products 2,4-DTBP and 2,6-DTBP, which are more widely used antioxidants.[2]

Synthese von 2,4,6-Tri-tert-butylphenol mit Isobuten
Synthese von 2,4,6-Tri-tert-butylphenol mit Isobuten

A synthesis of 2,4,6-tri-tert-butylphenol has been described that is also suitable as a teaching experiment. Methyl tert-butyl ether is used as the alkylating agent and sulfuric acid as catalyst. 2,4,6-TTBP is being obtained in 69% yield.[6]

Synthese von 2,4,6-TTBP mit Methyl-tert-butylether (MTBE)
Synthese von 2,4,6-TTBP mit Methyl-tert-butylether (MTBE)

Properties

2,4,6-Tri-tert-butylphenol is a white solid which dissolves in many organic solvents, but not in aqueous or alcoholic alkaline solutions. The green-blue coloring with iron(III)chloride, which is characteristic for phenols, does not occur in 2,4,6-TTBP. The compound is oxidizable in air but practically non-biodegradable.[7]

As an electron-rich aromatic, 2,4,6-tri-tert-butylphenol can also be easily oxidized electrochemically.[8] In the alkaline, the phenolate anion formed is first oxidized in a reversible reaction to the phenoxy radical. The stable radical is oxidized by further electron withdrawal to the phenoxonium cation, which reacts in water to give 2,4,6-tri-tert-butyl-4-hydroxy-2,5-cyclohexadienone.

Elektrochemische Oxidation von 2,4,6-TTBP
Elektrochemische Oxidation von 2,4,6-TTBP

In acidic media, the hydroxydienone is dealkylated with the cleavage of the tert-butyl group in the 4-position to the 2,6-di-tert-butylhydroquinone, which is oxidized to the end product 2,6-di-tert-butyl-1,4-benzoquinone.

Dealkylierung zum 1,4-Benzochinon
Dealkylierung zum 1,4-Benzochinon

The oxidation of 2,4,6-tri-tert-butylphenol in the alkaline to the intensely blue-colored phenoxy radical can also occur with potassium ferricyanide.[1][9][6] The 2,4,6-tri-tert-butylphenoxy radical forms blue crystals on cooling to -70 °C which are stable at room temperature for several weeks and only gradually turn yellow.[9] The phenoxy radical reacts with oxygen as a diradical to form a 4,4'-linked peroxide forming yellow crystals.[10]

Oxidation von 2,4,6-TTBP mit Hexacyanoferrat (III) zum Peroxid
Oxidation von 2,4,6-TTBP mit Hexacyanoferrat (III) zum Peroxid

Applications

The electron-rich 2,4,6-tri-tert-butylphenol can easily be oxidized to the phenoxy radical, which in the 4-position adds phenols,[11][12] as well as alcohols and thiols[13] to the corresponding cyclohexadienones. The cyclohexadienones, also referred to in the literature as Chinolether, cleave the 4-position tert-butyl group upon heating under acidic conditions and aromatizes back to the substituted phenol.

The reaction can be used for the synthesis of 2,6-di-tert-butyl-4-methoxyphenol, which is frequently used as an antioxidant.

Synthese von 2,6-Di-tert-butyl-4-methoxyphenol aus 2,4,6-TTBP
Synthese von 2,6-Di-tert-butyl-4-methoxyphenol aus 2,4,6-TTBP

2,4,6-TTBP is used as stabilizers, free-radical scavengers and antioxidants in technical applications, such as in fuels, hydraulic fluids and lubricating oils, as well as in elastomeric and thermoplastic polymers. Because of its pronounced persistence, its high tendency for bioaccumulation and aquatic toxicity, 2,4,6-TTBP is only of low industrial use and is even forbidden, for example, in Japan.

The phenoxy radical of 2,4,6-TTBP is also described as a sterically demanding protecting group in a reagent for the transfer of a nucleophilic dimethylaminomethyl group [(CH3)2-N-CH2-] to form tertiary amines.[14]

References

  1. 1 2 Warren, J. J.; Tronic, T. A.; Mayer, J. M. (2010). "Thermochemistry of Proton-Coupled Electron Transfer Reagents and Its Implications". Chemical Reviews. 110 (12): 6961–7001. doi:10.1021/cr100085k. PMC 3006073. PMID 20925411.
  2. 1 2 Peter P. Klemchuk (2005). "Antioxidants". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a03_091. ISBN 978-3527306732.
  3. ↑ „auch in diesem Falle [findet] scheinbar eine directe Addition eines ungesättigten Kohlenwasserstoffs an eine aromatische Substanz statt“. W. Koenigs (1890), "Ueber Condensationen ungesättigter Kohlenwasserstoffe mit Phenolen", Chem. Ber. (in German), vol. 23, no. 2, pp. 3144–3146, doi:10.1002/cber.189002302257
  4. ↑ A.R. Hajipour; Y. Ghayeb; N. Sheikhan; A.E. Ruoho (2009), "Brønsted acidic ionic liquid as an efficient and reusable catalyst for one-pot synthesis of 1-amidoalkyl 2-naphthols under solvent-free conditions", Tetrahedron Lett., vol. 50, no. 40, pp. 5649–5651, doi:10.1016/j.tetlet.2009.07.116
  5. ↑ G.H. Stillson; D.W. Sawyer; C.K. Hunt (1945), "The hindered phenols", J. Am. Chem. Soc., vol. 67, no. 2, pp. 303–307, doi:10.1021/ja01218a045
  6. 1 2 B.G. Somers; C.D. Cook (1955), "The preparation of 2,4,6-tri-tert-butylphenol", J. Chem. Educ., vol. 32, no. 6, p. 312, doi:10.1021/ed032p312
  7. ↑ "Screening Assessment for the Challenge, Phenol, 2,4,6-tris(1,1-dimethylethyl)-(2,4,6-tri-tert-butylphenol), CAS Registry Number 732-26-3" (PDF). Environment Canada, Health Canada. November 2008. Retrieved 2017-01-11.
  8. ↑ J.A. Richards; P.E. Whitson; D.H. Evans (1975), "Electrochemical oxidation of 2,4,6-tri-tert-butylphenol", J. Electroanal. Chem. (in German), vol. 63, no. 3, pp. 311–327, doi:10.1016/s0022-0728(75)80303-2
  9. 1 2 C.D. Cook; D.A. Kuhn; P. Fianu (1956), "Oxidation of hindered phenols. IV. Stable phenoxy radicals", J. Am. Chem. Soc., vol. 78, no. 9, pp. 2002–2005, doi:10.1021/ja01590a067
  10. ↑ C.D. Cook; R.C. Woodworth (1953), "Oxidation of hindered phenols. II. The 2,4,6-Tri-t-butylphenoxy radical", J. Am. Chem. Soc., vol. 75, no. 24, pp. 6242–6244, doi:10.1021/ja01120a040
  11. ↑ US 3410878, H.-D. Becker, "Preparation of quinol ethers", issued 1968-11-12
  12. ↑ E. Müller; K. Ley; G. Schlechte (1957), "Über Sauerstoffradikale, VIII. Über Dehydrierung von Phenolen", Chem. Ber. (in German), vol. 90, no. 11, pp. 2660–2672, doi:10.1002/cber.19570901136
  13. ↑ US 3895069, J.H. Atkinson, D. Clark, "Process for the preparation of 2,4,6-trialkyl-4-alkylthio or 4-alkoxycyclohexadi-2,5-ene-1-ones", issued 1975-7-15
  14. ↑ D. Seebach; T. Hassel (1978), "2,4,6-Tri-tert-butylphenoxy (TBPO) als sterisch wirksame Carbonylschutzgruppe — Ein neues nucleophiles Dimethylaminomethylierungsmittel", Angew. Chem. (in German), vol. 90, no. 4, pp. 296–297, doi:10.1002/ange.19780900422
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.