H3PW12O40 Anchored on the Three-Dimensional and Networked SBA-15 as an Efficient and Recyclable Catalyst for Mannich Reaction

Authors

  • Tengfei Zhang Key Laboratory of Low Carbon Energy and Chemical Engineering, College of Chemical and Environmental Engineering, Shandong University of Science and Technology, Qingdao Shandong
  • Wei Zhang
  • Hao Dong
  • Qing Liu

DOI:

https://doi.org/10.29356/jmcs.v64i1.1034

Keywords:

H3PW12O40, 3D-SBA-15, heterogeneous catalysis, Mannich reaction

Abstract

Abstract. The three-dimensional and networked SBA-15 (3D-SBA-15) supported phosphotungstic acid (PW) was used as heterogeneous catalyst for the one-pot three-components Mannich reaction at room temperature. The H3PW12O40/3D-SBA-15 catalyst was prepared using an impregnation method and confirmed by series of characterizations such as Fourier-transform infrared spectra (FT-IR), scanning electron microscope (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), N2 physisorption and thermogravimetric (TG) analysis. 50PW/3D-SBA-15 catalyst with H3PW12O40 loading of 50 wt% showed the highest yield of 93% in 1.8 h for the Mannich reaction of benzaldehyde, aniline and acetophenone under solvent-free condition. A series of β-aminoketone derivatives were synthesized successfully in the presence of this catalyst. In addition, H3PW12O40/3D-SBA-15 catalyst can be easily recovered and reused four times without significant decrease of the activity. This work provides an improved modification of the three-component Mannich reaction in terms of mild reaction conditions, clean reaction profiles, small quantity of catalyst and a simple workup procedure.

                                              

Resumen.  El ácido fosfotungstico (PW) se soportó en sílice SBA-15 (3D-SBA-15) y se usó como catalizador heterogéneo en la reacción de Mannich en un solo paso de tres componentes a temperatura ambiente. El catalizador H3PW12O40/3D-SBA-15 se preparó mediante impregnación y se caracterizó por espectroscopia de infrarrojo (FT-IR), microscopia electrónica de barrido (SEM), microscopía electrónica de transmisión (TEM), difracción de rayos-X (XRD), fisisorción de N2 y análisis termogravimétrico (TG). El catalizador 50PW/3D-SBA-15, con una carga de H3PW12O40 del 50% en peso, mostró el rendimiento más alto del 93% en 1.8 h para la reacción de Mannich entre benzaldehído, anilina y acetofenona, sin disolvente. Se sintetizó una serie de derivados de β-aminocetona en presencia de este catalizador. Además, el catalizador H3PW12O40/3D-SBA-15 puede recuperarse fácilmente y reutilizarse cuatro veces sin pérdida significativa de la actividad. Este trabajo reporta una modificación de la reacción de Mannich de tres componentes bajo condiciones de reacción suaves, perfiles de reacción limpios, pequeña cantidad de catalizador y un procedimiento de tratamiento simple.

Downloads

Download data is not yet available.

References

Vaccaro, L. Beilstein J. Org. Chem. 2016, 12, 2763-2765. DOI: https://doi.org/10.3762/bjoc.12.273

Rafiee, E.; Eavani, S. Green Chem. 2011, 13, 2116. DOI: https://doi.org/10.1039/c1gc15291b

Yang, H.; Dong, H.; Zhang, T.; Zhang, Q.; Zhang, G.; Wang, P.; Liu, Q. Catal. Lett. 2018, 149, 778-787. DOI: https://doi.org/10.1007/s10562-018-2632-9

Yang, L.; Xu, L.W.; Xia, C.G. Tetrahedron Lett. 2005, 46, 3279-3282. DOI: https://doi.org/10.1016/j.tetlet.2005.03.112

Yan, X.; Chen, J.; Xue, Q.; Miele, P. Micropor. Mesopor. Mat. 2010, 135, 137-142. DOI: https://doi.org/10.1016/j.micromeso.2010.07.001

Hussain, M.; Liu, J.; Zhang, Z.; Hu, M.; Li, Y.; Min, X. ChemistrySelect 2018, 3, 8787-8792.

Yeszhanov, A.B.; Mashentseva, A.A.; Korolkov, I.V.; Gorin, Y.G.; Kozlovskiy, A.L.; Zdorovets, M.V. Chem. Pap. 2018, 72, 3189-3194. DOI: https://doi.org/10.1007/s11696-018-0539-y

Pettignano, A.; Bernardi, L.; Fochi, M.; Geraci, L.; Robitzer, M.; Tanchoux, N.; Quignard, F. New J. Chem. 2015, 39, 4222-4226. DOI: https://doi.org/10.1039/C5NJ00349K

Sawant, D.P.; Justus, J.; Balasubramanian, V.V.; Ariga, K.; Srinivasu, P.; Velmathi, S.; Halligudi, S.B.; Vinu, A. Chem. 2008, 14, 3200-3212. DOI: https://doi.org/10.1002/chem.200701562

Okuhara, T.; Mizuno, N.; Misono, M. Appl. Catal. A-Gen. 2001, 222, 63-77. DOI: https://doi.org/10.1016/S0926-860X(01)00830-4

Rafiee, E.; Joshaghani, M.; Eavani, S.; Rashidzadeh, S. Green Chem. 2008, 10, 982-989. DOI: https://doi.org/10.1039/b803249a

Sahoo, S.; Joseph, T.; Halligudi, S.B. J. Mol. Catal. A: Chem. 2006, 244, 179-182. DOI: https://doi.org/10.1016/j.molcata.2005.09.012

Zhang, Y.; Zhao, Y.; Xia, C. J. Mol. Catal. A: Chem. 2009, 306, 107-112. DOI: https://doi.org/10.1016/j.molcata.2009.02.032

Zhang, H.; Mifsud, M.; Tanaka, F.; Barbas Iii, C.F. J. Am. Chem. Soc. 2006, 128, 9630-9631. DOI: https://doi.org/10.1021/ja062950b

Timofeeva, M.N. Appl. Catal. A-Gen 2003, 256, 19-35. DOI: https://doi.org/10.1016/S0926-860X(03)00386-7

Wang, Y.; Satyavolu, N.S.R.; Lu, Y. Curr. Opin. Colloid Interface Sci. 2018, 38, 158-169. DOI: https://doi.org/10.1016/j.cocis.2018.10.009

Chen, G.; Zhang, X.; Guo, C.; Yuan, G. Russ. J. Phys. Chem. A 2010, 84, 2247-2253. DOI: https://doi.org/10.1134/S0036024410130078

Hu, B.; Liu, H.; Tao, K.; Xiong, C.; Zhou, S. J. Phys. Chem. C 2013, 117, 26385-26395. DOI: https://doi.org/10.1021/jp4098028

Dong, C.; Li, X.; Wang, A.; Chen, Y.; Liu, H. Catal. Commun. 2017, 100, 219-222. DOI: https://doi.org/10.1016/j.catcom.2017.07.003

Dan, H.; Dong, X.; Lu, X.; Ding, Y. J. Sol-Gel Sci. Technol. 2017, 81, 782-790. DOI: https://doi.org/10.1007/s10971-016-4227-5

Schwanke, A.; Favero, C.; Balzer, R.; Bernardo-Gusmão, K.; Pergher, S. J. Braz. Chem. Soc. 2017, 29,328-333.

Yang, Q.; Gu, F.; Tang, Y.; Zhang, H.; Liu, Q.; Zhong, Z.; Su, F. RSC Adv. 2015, 5, 26815-26822. DOI: https://doi.org/10.1039/C4RA16832A

Zhou, Y.; Lin, W.G.; Yang, J.; Gao, L.; Lin, N.; Yang, J.Y.; Hou, Q.; Wang, Y.; Zhu, J.H. J. Colloid Interface Sci. 2011, 364, 594-604. DOI: https://doi.org/10.1016/j.jcis.2011.08.061

Liu, Q.; Tian, Y. Int. J. Hydrogen Energy 2017, 42, 12295-12300. DOI: https://doi.org/10.1016/j.ijhydene.2017.02.070

Cele, Z.E.D.; Pawar, S.A.; Naicker, T.; Maguire, G.E.M.; Arvidsson, P.I.; Kruger, H.G.; Govender, T. Eur. J. Org. Chem. 2014, 2014, 2253-2260. DOI: https://doi.org/10.1002/ejoc.201301823

Liu, Q.; Zhang, Z. Catal. Sci. Technol. 2019, 9, 4821-4834. DOI: https://doi.org/10.1039/C9CY01028A

Wang, H.; Gao, X.; Wang, Y.; Wang, J.; Niu, X.; Deng, X. Ceram. Int. 2012, 38, 6931-6935. DOI: https://doi.org/10.1016/j.ceramint.2012.05.062

Kooti, M.; Kooshki, F.; Nasiri, E.; Sedeh, A.N. J. Iran. Chem. Soc. 2018, 15, 943-953. DOI: https://doi.org/10.1007/s13738-018-1292-4

Armatas, G.S.; Katsoulidis, A.P.; Petrakis, D.E.; Pomonis, P.J. J. Mater. Chem. 2010, 20, 8631-8638. DOI: https://doi.org/10.1039/c0jm01283a

Zhu, X.; Chen, C.; Yu, B.; Wu, Y.; Zhang, G.; Zhang, W.; Gao, Z. Catal. Sci. Technol. 2015, 5, 4346-4349. DOI: https://doi.org/10.1039/C5CY00793C

Hussain, M.; Liu, J.; Zhang, Z.; Hu, M.; Li, Y.; Min, X. ChemistrySelect 2018, 3, 8787-8792. DOI: https://doi.org/10.1002/slct.201801064

Gawande, M.B.; Velhinho, A.; Nogueira, I.D.; Ghumman, C.A.A.; Teodoro, O.M.N.D.; Branco, P.S. RSC Adv. 2012, 2, 6144-6149. DOI: https://doi.org/10.1039/c2ra20955a

Eftekhari-Sis, B.; Hashemi, M.M.; Farmad, F. Synth. Commun. 2009, 39, 4441-4453. DOI: https://doi.org/10.1080/00397910902906594

Azizi, N.; Torkiyan, L.; Saidi, M.R. Org. Lett. 2006, 8, 2079-2082. DOI: https://doi.org/10.1021/ol060498v

×

Additional Files

Published

2019-12-12

Issue

Section

Regular Articles
x

Similar Articles

<< < 8 9 10 11 12 13 14 15 16 17 > >> 

You may also start an advanced similarity search for this article.

Loading...