In(OTf)3-catalyzed synthesis of 2-styryl quinolines: scope and limitations of metal Lewis acids for tandem Friedländer annulation–Knoevenagel condensation. Issue 4 (9th December 2014)

• Record Type: Journal Article
• Authors: Kumar, Dinesh; Kumar, Asim; Qadri, Mohammad Mohsin; Ansari, Md. Imam; Gautam, Abhishek; Chakraborti, Asit K.
• Is Part Of: RSC advances. Volume 5:Issue 4(2015)
• Page Start: 2920
• Page End: 2927
• Publication Date: 2014-12-09
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/c4ra10613j
• Languages: English
• ISSNs: 2046-2069

Abstract

Abstract : Investigation of metal Lewis acids for one-pot tandem Friedländer annulation–Knoevenagel condensation and exploration of In(OTf)3 for synthesis of 2-styryl quinolines. Abstract : The catalytic potential of different metal Lewis acids has been assessed for the one-pot tandem Friedländer annulation and Knoevenagel condensation involving 2-aminobenzophenone, ethyl acetoacetate, and benzaldehyde to form 2-styryl quinoline under solvent free conditions. While various metal Lewis acids were effective in promoting the Friedländer annulation step, In(OTf)3 was the only effective catalyst for the subsequent Knoevenagel condensation reaction suggesting In(OTf)3 as the stand-alone catalyst for the tandem Friedländer–Knoevenagel reaction to form 2-styryl quinolines. The protocol is compatible with different variations of aromatic/hetero-aromatic aldehydes and α, β unsaturated aromatic aldehydes giving highly functionalized 2-aryl/heteroaryl vinyl quinolines. The catalyst can be recovered and reused to afford the desired product in very good to excellent yields.