The catalytic activity of gel and macroreticular ion-exchange resins (Lewatit and Amberlyst-15) was evaluated for the reaction of benzene with benzyl alcohol and benzyl chloride at 80°C in the liquid phase. With benzyl chloride, the monobenzylation product, diphenylmethane, was obtained in low yield
Alkylation of toluene with aliphatic alcohols and 1-octene catalyzed by cation-exchange resins
✍ Scribed by Elizabeth Roditi Lachter; Rosane Aguiar da Silva San Gil; David Tabak; Valéria Gonçalves Costa; Cristiane P.S Chaves; Jaqueline Araújo dos Santos
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- English
- Weight
- 252 KB
- Volume
- 44
- Category
- Article
- ISSN
- 1381-5148
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📜 SIMILAR VOLUMES
polymers used in the present study was between tertachloromethane and methanol on comparison of the values obtained with small molecules. It was also made clear that membrane polarity can explain the membrane phenomena.
The corresponding 2-furylhetarylmethanes were obtained by the reaction of furan, thiophene, or pyrrole with furfuryl alcohol in the presence of the strongly acidic Amberlyst 15 cation-exchange resin in the H + form. The alkylation of furan and thiophene takes place regiospecifically in the 2position
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