Abstract
Study of the catalytic ethylation of p-t-butyltoluene in the presence of organosodium compounds, and of toluene in the presence of organopotassium compounds, was carried out at an ethylene pressure of 40 bar. Various yields of different products were obtained after 23 h of reaction in the presence of different tertiary polyamines used to complex and solubilize the organoalkali compounds. A higher initial ethylation rate was observed in the presence of organosodium than in the presence of organopotassium species. However, the thermal stability of organopotassium species being higher, much higher yields were observed in their presence in catalytic ethylation reactions than those observed previously. The results obtained concerning metallation or ethylation of hindered alkylaromatics may be interpreted by an anionic mechanism and the activation by a steric effect.
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