Issue 2, 2011

Ruthenium(iv)catalysts for the selective estragole to trans-anetholeisomerization in environmentally friendly media

Abstract

Several ruthenium(IV) complexes have been tested as potential catalysts for the isomerization of estragole into anethole using water and glycerol as alternative green reaction media. Best results in terms of activity and E-selectivity were obtained with the dimeric species [{RuCl(μ-Cl)(η3:η3-C10H16)}2] (C10H16 = 2,7-dimethylocta-2,6-diene-1,8-diyl) and the mononuclear derivative [RuCl2(η3:η3-C10H16){P(OMe)3}]. In particular, using a ruthenium loading of 1 mol%, almost quantitative and stereoselective formation of trans-anethole (trans/cis ratios = 99 : 1) could be reached at 80 °C in short times (5–30 min) employing waterMeOH (EtOH) or glycerolMeOH (EtOH) mixtures (1 : 1 v/v) as solvent. Recyclability issues have also been addressed.

Graphical abstract: Ruthenium(iv) catalysts for the selective estragole to trans-anethole isomerization in environmentally friendly media

Supplementary files

Article information

Article type
Paper
Submitted
09 Aug 2010
Accepted
23 Nov 2010
First published
20 Dec 2010

Green Chem., 2011,13, 307-313

Ruthenium(IV) catalysts for the selective estragole to trans-anethole isomerization in environmentally friendly media

B. Lastra-Barreira, J. Francos, P. Crochet and V. Cadierno, Green Chem., 2011, 13, 307 DOI: 10.1039/C0GC00417K

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