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Synthesis of phenolic antioxidants with isobornyl and tert-butyl fragments

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Abstract

Hybrid antioxidants, phenols with a terpene and tert-butyl substituents, were synthesized by the alkylation of 2-tert-butyl-4-methylphenol with camphene and 2-isobornylphenol with tert-butyl chloride in the presence of acidic heterogeneous catalysts, montmorillonite KSF and FIBAN K-1. Antioxidant activity of the synthesized terpenophenols was evaluated using spectrophotometry.

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Authors and Affiliations

  1. Institute of Chemistry, Komi Scientific Center, Ural Branch, Russian Academy of Sciences, ul. Pervomaiskaya 48, Syktyvkar, 167982, Russia

    I. V. Fedorova, I. Yu. Chukicheva, O. A. Shumova & A. V. Kutchin

Authors
  1. I. V. Fedorova
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  2. I. Yu. Chukicheva
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  3. O. A. Shumova
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  4. A. V. Kutchin
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Corresponding author

Correspondence to I. Yu. Chukicheva.

Additional information

Original Russian Text © I.V. Fedorova, I.Yu. Chukicheva, O.A. Shumova, A.V. Kutchin, 2013, published in Zhurnal Obshchei Khimii, 2013, Vol. 83, No. 6, pp. 972–979.

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Fedorova, I.V., Chukicheva, I.Y., Shumova, O.A. et al. Synthesis of phenolic antioxidants with isobornyl and tert-butyl fragments. Russ J Gen Chem 83, 1103–1110 (2013). https://doi.org/10.1134/S1070363213060170

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  • DOI: https://doi.org/10.1134/S1070363213060170

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