Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
231366 | The Journal of Supercritical Fluids | 2011 | 5 Pages |
Environmentally benign, non-catalytic, simple, and complete aromatic ring methylation of catechol derivatives by using 1,3,5-trioxane as the source of methyl groups was investigated in subcritical and supercritical water and under solvent-free conditions. Irrespective of the presence of subcritical and supercritical water as a reaction medium, catechol and 4-methylcatechol afforded the permethylation product 3,4,5,6-tetramethylcatechol. Only a small amount of 3,4,5,6-tetramethylcatechol (2% yield) was obtained under solvent-free conditions at 400 °C for 10 min. However, supercritical water considerably accelerated the formation of 3,4,5,6-tetramethylcatechol (13% yield) under the conditions of 400 °C, 10 min, and 0.35 g/mL water density.
Graphical abstractFigure optionsDownload full-size imageDownload as PowerPoint slideHighlights► An environmentally benign, simple, non-catalytic method for permethylation of catechol derivatives in subcritical and supercritical water. ► The temperature, reaction time, and water density dependence of permethylation of catechol derivatives. ► Permethylation of catechol derivatives in a very short reaction time (10 min) under the conditions of 400 °C and 0.35 g/mL water density in supercritical water.