Issue 9, 2012

One-pot solvent-free synthesis of quinolines by C–H activation/C–C Bond formation catalyzed by recyclable iron(iii) triflate

Abstract

A novel application of highly stable Fe(OTf)3 as an efficient catalyst for carbon–carbon bond formation via the activation of a terminal alkyne C–H bond under solvent-free conditions is described. Notably, this protocol of green synthesis, which produced quinolines from the reaction of amines, aldehydes and terminal aryl alkynes, shows attractive characteristics including concise one-pot conditions, high atom economy, very limited energy consumption, and the sequential catalytic process requires only a catalytic (5 mol%) amount of Fe(OTf)3 with short reaction periods (3 h). Meanwhile, the catalyst was easily recovered from the reaction system and reused smoothly with only a little loss of activity.

Graphical abstract: One-pot solvent-free synthesis of quinolines by C–H activation/C–C Bond formation catalyzed by recyclable iron(iii) triflate

Supplementary files

Article information

Article type
Paper
Submitted
27 Jan 2012
Accepted
30 Jan 2012
First published
30 Jan 2012

RSC Adv., 2012,2, 3759-3764

One-pot solvent-free synthesis of quinolines by C–H activation/C–C Bond formation catalyzed by recyclable iron(III) triflate

C. Yao, B. Qin, H. Zhang, J. Lu, D. Wang and S. Tu, RSC Adv., 2012, 2, 3759 DOI: 10.1039/C2RA20172K

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