Oligomerization of 3,5-dimethyl benzyl alcohol promoted by clay: experimental and theoretical study

Molecules. 2010 Nov 11;15(11):8156-68. doi: 10.3390/molecules15118156.

Abstract

Linear oligomerization of 3,5-dimethyl benzyl alcohol is induced by a montmorillonite clay (Tonsil Optimum Extra), producing 1,3,5,7-tetramethyl-9,10-dihydro-anthracene, which, by loss of protons results in the product 1,3,5,7-tetramethylanthracene. It was also found that the compounds 4-(3´,5´-dimethylbenzyl)-1,3,5,7-tetramethyl-9,10-dihydroanthracece and 4-(3´,5´-dimethylbenzyl)-1,3,5,7-tetra-methylanthracene were formed from 1,3,5,7-tetramethyl-9,10-dihydroanthracene. 1,3,5,7-Tetramethylanthryl radical cation was formed from 1,3,5,7-tetramethyl-9,10-dihydroanthracene; it was characterized by Electronic Paramagnetic Resonance (EPR). On the other hand, a theoretical analysis was performed, allowing the rationalization of the observed products and some of the key reaction steps.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Bentonite / chemistry*
  • Benzyl Alcohol / chemistry*
  • Electron Spin Resonance Spectroscopy
  • Molecular Structure
  • Polymerization

Substances

  • Bentonite
  • Benzyl Alcohol