Issue 9, 2014

Carbon-supported iron–ionic liquid: an efficient and recyclable catalyst for benzylation of 1,3-dicarbonyl compounds with alcohols

Abstract

The effect of the addition of ILs with non-coordinating anions on the iron-catalyzed benzylation of 1,3-dicarbonyl compounds with alcohols under solvent free conditions has been evaluated. Among them, the presence of those containing the bistriflimide anion was found to be crucial for selectivity towards the benzylated product in a homogenous reaction. Therefore, the catalytic activity of Fe(OTf)3–N4111NTf2 combination supported on carbon materials with different textural and chemical surface properties has been studied. In the heterogeneous phase, reaction selectivity was also enhanced by the addition of the IL. However, substantial differences between the activities of different Fe-IL/carbon material catalytic systems were observed, indicating the influence of carbon support properties. With regards to selectivity, the best results were obtained using carbon supports with low microporosity. Moreover, the presence of oxygen functional groups on the carbon surface improved catalyst recycling.

Graphical abstract: Carbon-supported iron–ionic liquid: an efficient and recyclable catalyst for benzylation of 1,3-dicarbonyl compounds with alcohols

Supplementary files

Article information

Article type
Paper
Submitted
28 Apr 2014
Accepted
01 Jul 2014
First published
08 Jul 2014

Green Chem., 2014,16, 4306-4311

Author version available

Carbon-supported iron–ionic liquid: an efficient and recyclable catalyst for benzylation of 1,3-dicarbonyl compounds with alcohols

P. Moriel and A. B. García, Green Chem., 2014, 16, 4306 DOI: 10.1039/C4GC00755G

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