Alkylation of Aromatic Compounds in the Presence of Catalysts Based on Mesoporous Phenol–Formaldehyde Polymers
- Authors: Boronoev M.P.1, Gotszyun M.1, Talanova M.Y.1, Karakhanov E.A.1
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Affiliations:
- Faculty of Chemistry
- Issue: Vol 58, No 5 (2018)
- Pages: 412-417
- Section: Article
- URL: https://journals.rcsi.science/0965-5441/article/view/180177
- DOI: https://doi.org/10.1134/S0965544118050043
- ID: 180177
Cite item
Abstract
A catalyst based on a mesoporous phenol–formaldehyde polymer (MPF) as an organic support modified with the IMHSO4 ionic liquid has been synthesized. The catalytic activity of the sample has been studied in the alkylation of aromatic compounds with octene-1. It has been found that the use of the catalyst in phenol alkylation leads to the formation of both alkylphenols (C-alkylates) and alkyl phenyl ethers (O-alkylates) with a total yield of up to 60%. In the case of alkylation of benzene and benzene derivatives, significant conversion values (45–50%) are achieved only for toluene and anisole.
About the authors
M. P. Boronoev
Faculty of Chemistry
Email: kar@petrol.chem.msu.ru
Russian Federation, Moscow
Ma Gotszyun
Faculty of Chemistry
Email: kar@petrol.chem.msu.ru
Russian Federation, Moscow
M. Yu. Talanova
Faculty of Chemistry
Email: kar@petrol.chem.msu.ru
Russian Federation, Moscow
E. A. Karakhanov
Faculty of Chemistry
Author for correspondence.
Email: kar@petrol.chem.msu.ru
Russian Federation, Moscow
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