For Libraries For Publication Open Access Downloads About Us Contact Us
Paper Titles
Continuous Catalytic Hydrogenation of Carbon Dioxides on Immobilized Ru Functionalistic Catalysts
p.227
The Benzoin Condensation Reaction in the Presence of the Ultrasonic
p.235
Investigation on Synthesis Conditions of Silicon-Doped Hydrotalcite-Like Compounds
p.239
Adsorption of Benzothiophene on Activated Carbon Supported Copper and Palladium
p.243
An Efficient One-Pot Four-Component Hantzsch Reaction to Prepare Hydroquinolines Catalyzed by a Poly(ethylene glycol) Bridged Dicationic Basic Ionic Liquid under Solvent-Free Conditions
p.247
Ethylenediamine Catalyzed Decarboxylation of Oxaloacetic Acid: A DFT Investigation
p.253
A Simple Procedure for the Esterification and Transesterification Using p-Toluene Sulfonic Acid as Catalyst
p.259
Synthesis, Characterization and Properties of Tri-n-octylmethyl-ammonium Methyl Carbonate
p.263
Synthesis of 2-Pyridyl Tribromomethyl Sulfone
p.272

An Efficient One-Pot Four-Component Hantzsch Reaction to Prepare Hydroquinolines Catalyzed by a Poly(ethylene glycol) Bridged Dicationic Basic Ionic Liquid under Solvent-Free Conditions

Article Preview

Abstract:

A piperidine-functionalized poly (ethylene glycol) bridged dicationic ionic liquid PEG800-DPIL(Cl) was synthesized and applied to catalyze the four-component Hantzsch reaction under solvent-free conditions and afford hydroquinolines with high to excellent yields. PEG800-DPIL(Cl) could be recovered by simple workup and recycled for at least eight times without obvious activity loss.

You might also be interested in these eBooks
Advances in Chemical Engineering III View Preview

Info:

Periodical:

Advanced Materials Research (Volumes 781-784)

Pages:

247-252

DOI:

https://doi.org/10.4028/www.scientific.net/AMR.781-784.247

Citation:

Cite this paper

Online since:

September 2013

Authors:

Jun Luo*, Tan Tan Xing, Ying Lei Wang, Jian Feng Ju

Keywords:

Hydroquinolines, Ionic Liquid (IL), Multicomponent Reaction, Solvent-Free Conditions, Supported Catalyst

Export:

RIS, BibTeX

Price:

Permissions CCC:

Request Permissions

Permissions PLS:

Request Permissions

Сopyright:

© 2013 Trans Tech Publications Ltd. All Rights Reserved

Share:

Citation:

* - Corresponding Author

References

[1] (a) A. Domling, W. Wang and K. Wang: Chem. Rev. Vol. 112 (2012), p.3083; (b) M.S. Singh and S. Chowdhury: RSC Adv. Vol. 2 (2012), p.4547; (c) Y.L. Gu: Green Chem. Vol. 14 (2012), p. (2091).

Google Scholar

[2] (a) T. Godfaid, R. Miller and M. Wibo: Pharmacol. Rev. Vol. 38 (1986).

Google Scholar

[3] (a) X.L. Liao, W.B. Lin and J. Lu: Tetrahedron Lett. Vol. 51 (2010).

Google Scholar

[4] L. Shen, S. Cao, J.J. Wu, H. Li, J. Zhang, M.X. Wu and X.H. Qian: Tetrahedron Lett. Vol. 51 (2010), p.4866.

Google Scholar

[5] A. Debache, W. Ghalem and R. Boulcina: Tetrahedron Lett. Vol. 50 (2009), p.5248.

Google Scholar

[6] (a) S.R.C. Herkupally and R.M. Ekala: Chem. Pharm. Bull. Vol. 56 (2008), p.1002; (b) H.N. Peng, X.M. Peng and D.G. Zheng: Asian J. Chem. Vol. 23 (2011), p.1833.

Google Scholar

[7] R. Sridhar and P.T. Perumal: Tetrahedron Vol. 61 (2005), p.2465.

Google Scholar

[8] A.G. Sathicq, G.P. Romanelli, A. Ponzinibbio, G.T. Baronetti and H.J. Thomas: Lett. Org. Chem. Vol. 7 (2010), p.511.

Google Scholar

[9] J. Safari, S.H. Banitaba and S.D. Khalili: J. Mol. Catal. A: Chem. Vol. 335 (2011), p.46.

Google Scholar

[10] C.G. Evans and J.E. Gestwicki: Org. Lett. Vol. 11 (2009), p.2957.

Google Scholar

[11] V. Sivamurugan, A. Vinu, M. Palanichamy and V. Murugesan: Heteroatom. Chem. Vol. 17 (2006), p.267.

Google Scholar

[12] L. Shen, S. Cao and J.J. Wu: Tetrahedron Lett. Vol. 51 (2010), p.4866.

Google Scholar

[13] (a) A. Kumar and R.A. Maurya: Tetrahedron Vol. 63 (2007), p.1946; (b) D.R.B. Ducatti, A. Massi, M.D. Noseda, M.E.R. Duarte and A. Dondoni: Org. Biomol. Chem. Vol. 7 (2009), p. (1980).

Google Scholar

[14] (a) L.M. Wang, J. Shang and L. Zhang: Tetrahedron Vol. 61 (2005), p.1539; (b) J.L. Donelson, R.A. Gibbs and S.K. De: J. Mol. Catal. A: Chem. Vol. 256 (2006), p.309.

Google Scholar

[15] (a) S.K. Ko and C.F. Yao: Tetrahedron Vol. 62 (2006), p.7293; (b) V. Sridharan and P.T. Perumal: Tetrahedron Vol. 63 (2007), p.4407.

Google Scholar

[16] K.K. Pasunooti, C.N. Jensen and H. Chai: J. Comb. Chem. Vol. 12 (2010), p.577.

Google Scholar

[17] E. Mosaddegh and A. Hassankhani: Arab. J. Chem. (2010), p.1.

Google Scholar

[18] M. Hong, C. Cai and W.B. Yi: J. Fluorine Chem. Vol. 131 (2010), p.111.

Google Scholar

[19] C.A. Antonyraj and S. Kannan: Appl. Catal. A: Gen. Vol. 338 (2008), p.121.

Google Scholar

[20] (a) M. Li, W.S. Guo and L.R. Wen: J. Mol. Catal. A: Chem. Vol. 258 (2006).

Google Scholar

[21] (a) M.Z. Kassaee, H. Masrouri and F. Movahedi: Monatsh. Chem. Vol. 141 (2010).

Google Scholar

[22] A. Kumar and R.A. Maurya: Tetrahedron Lett. Vol. 48 (2007), p.3887.

Google Scholar

[23] J.L. Wang, B.K. Liu and C. Yin: Tetrahedron Vol. 67 (2011), p.2689.

Google Scholar

[24] (a) M. Li, Z.Q. Zuo, L.R. Wen and S.W. Wang: J. Comb. Chem. Vol. 10 (2008).

Google Scholar

[25] (a) E. Ruiz, H. Rodriguez, J. Coro, E. Salfran, M. Suarez, R. Martinez-Alvarez and N. Martin: Ultrason. Sonochem. Vol. 18 (2011), p.32; (b) S.R. Guo and Y.Q. Yuan: Chin. Chem. Lett. Vol. 28 (2010), p.811.

Google Scholar

[26] A. Herath and N.D.P. Cosford: Org. Lett. Vol. 12 (2010), p.5182.

Google Scholar

[27] J.P. Hallett and T. Welton: Chem. Rev. Vol. 111 (2011), p.3508.

Google Scholar

[28] (a) H.Z. Zhi, C.X. Lü, Q. Zhang and J. Luo: Chem. Commun. Vol. 20 (2009).

Google Scholar

© 2025 Trans Tech Publications Ltd. All rights are reserved, including those for text and data mining, AI training, and similar technologies. For open access content, terms of the Creative Commons licensing CC-BY are applied.
Scientific.Net is a registered trademark of Trans Tech Publications Ltd.