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Reaction Kinetics, Mechanisms and Catalysis

, Volume 124, Issue 2, pp 711–725 | Cite as

Prins cyclization in 4-methyl-2-phenyl-tetrahydro-2H-pyran-4-ol preparation using smectite clay as catalyst

  • Eliška Vyskočilová
  • Anna Gruberová
  • Mariya Shamzhy
  • Eva Vrbková
  • Jiří Krupka
  • Libor Červený
Article

Abstract

Prins cyclization of isoprenol with benzaldehyde as a model aldehyde was performed using montmorillonite K10 as an acid catalyst. Various reaction conditions were used including catalyst modification by mineral acids and calcination. Both treatments influenced the selectivity to substituted tetrahydropyranol negatively. Due to the increased specific surface of the catalyst the reaction rate increased. Both addition of water and methanol to the reaction mixture prevented dehydration but the selectivity to desired product remained the same. Chosen reaction conditions (70 °C, ratio aldehyde:isoprenol 0.9:1, catalyst amount 110 wt%, solvent toluene) were used in Prins cyclization of other aldehydes with the similar results. Montmorillonite K10 may be used in preparation of substituted tetrahydropyranols with selectivity ranging from 59 to 69% (depending on aldehyde), which is comparable with or higher than heterogeneous catalysts used previously. This catalyst may be also used repeatedly with slight decrease in the reaction rate and no loss of selectivity.

Keywords

Prins cyclization Isoprenol Montmorillonite K10 Tetrahydropyranol 

Notes

Acknowledgement

This work was realized within the Operational Programme Prague—Competitiveness (CZ.2.16/3.1.00/24501) and “National Program of Sustainability“(NPU I LO1613) MSMT- 43760/2015.

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Copyright information

© Akadémiai Kiadó, Budapest, Hungary 2018

Authors and Affiliations

  1. 1.Department of Organic TechnologyUniversity of Chemistry and Technology PraguePrague 6Czech Republic
  2. 2.J. Heyrovský Institute of Physical ChemistryAcademy of Sciences of the Czech RepublicPrague 8Czech Republic

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