Tetrahedron letters

Synthesis of 1, 3-dialkylimidazolium-2-carboxylates by direct carboxylation of 1, 3-dialkylimidazolium chlorides with CO 2

I Tommasi, F Sorrentino

Index: Tommasi, Immacolata; Sorrentino, Fabiana Tetrahedron Letters, 2006 , vol. 47, # 36 p. 6453 - 6456

Full Text: HTML

Citation Number: 66

Abstract

1, 3-Dialkylimidazolium-2-carboxylates 1a and 1b are obtained in good to excellent yield and selectivity by carboxylation of the corresponding 1, 3-dialkylimidazolium chloride salts with a CO2/Na2CO3 system at temperatures ranging from 80 to 135° C. The effect of temperature and reaction time on the yield and the selectivity of the carboxylation products has been studied. Coupling the CO2-based synthesis of 1, 3-dialkylimidazolium-2- ...

Related Articles:

Betaine–Carbene Interconversions. From N-Ylides to Zwitterionic N-Heterocyclic Carbene–Borane Adducts

[Schmidt, Andreas; Beutler, Ariane; Albrecht, Marcel; Snovydovych, Bohdan; Ramirez, Francisco Javier Organic and Biomolecular Chemistry, 2008 , vol. 6, # 2 p. 287 - 295]

Novel synthon for incorporating 1, 3-dimethyl-imidazolium group into molecular architecture

[Berezin, Mikhail; Achilefu, Samuel Tetrahedron Letters, 2007 , vol. 48, # 7 p. 1195 - 1199]

More Articles...