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A ternary hybrid system based on combination of mesoporous silica, heteropolyacid and double-layered clay: an efficient catalyst for the synthesis of 2,4-dihydro-3H-pyrazol-3-ones and pyranopyrazoles in aqueous medium: studying the effect of the synthetic procedure on the catalytic activity

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Abstract

SBA/hydrotalcite/heteropolyacid nanocomposite is synthesized via a novel procedure in which the as-prepared heteropolyacid-loaded SBA-15 was impregnated with calcined hydrotalcite. The ternary hybrid system was characterized by using SEM/EDS, XRD, BET, TPD, TGA, FTIR and ICP-AES and also used as an efficient catalyst for the synthesis of 2,4-dihydro-3H-pyrazol-3-one derivatives via the reaction of arylaldehydes and 5-methyl-1H-pyrazol-3(2H)-one under reflux condition. Moreover, the catalytic activity of this catalyst was confirmed for the one-pot four-component reaction of aryl aldehydes, ethylacetoacetate, malononitrile and hydrazine hydrate/phenyl hydrazine in aqueous media for the synthesis of pyranopyroles. The investigation of the effect of the synthetic procedure and calcination of the hydrotalcite on the catalytic activity of the catalyst established that this factor does not exert a marked effect on the catalytic activity. The present procedures benefit from diverse advantages, including high yields, simplicity, mild reaction conditions and short reaction times. Moreover, this catalyst was reusable for up to five reaction runs and the HPA leaching was suppressed.

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References

  1. S. Rostamnia, E. Doustkhah, RSC Adv. 4, 28238 (2014)

    Article  CAS  Google Scholar 

  2. B. Karimi, F. Mansouri, M. Khorasani, Curr. Org. Chem. 20, 349 (2016)

    Article  CAS  Google Scholar 

  3. L. Konga, X. Zhoua, Y. Yaoa, P. Jiana, G. Diaoa, Environ. Technol. 37, 422 (2016)

    Article  Google Scholar 

  4. H. Veisi, A.A. Manesh, N. Eivazi, A.R. Faraji, RSC Adv. 5, 20098 (2015)

    Article  CAS  Google Scholar 

  5. H. Veisia, M. Hameliana, S. Hemmati, J. Mol. Catal. A Chem. 395, 25 (2014)

    Article  Google Scholar 

  6. A. Wach, M. Drozdek, B. Dudek, P. Latka, P. Kustrowski, Microporous Mesoporous Mater. 226, 433 (2016)

    Article  CAS  Google Scholar 

  7. X. Song, W. Zhu, K. Li, J. Wang, H. Niu, H. Gao, W. Gao, W. Zhang, J. Yu, M. Jia, Catal. Today 259, 59 (2016)

    Article  CAS  Google Scholar 

  8. S. Sadjadi, M.M. Heravi, RSC. Adv. 7, 30815 (2017)

    Article  CAS  Google Scholar 

  9. J. Zhang, P. Jiang, Y. Shen, W. Zhang, G. Bian, J. Porous Mater. 23, 431 (2016)

    Article  CAS  Google Scholar 

  10. V. Mahdavi, M. Mardani, Res. Chem. Intermed. 41, 8907 (2015)

    Article  CAS  Google Scholar 

  11. R.L. Oliveira, W. He, R.J.M. Klein Gebbink, K.P. de Jong, Catal. Sci. Technol. 5, 1919 (2015)

    Article  CAS  Google Scholar 

  12. D. Saikia, Y.-Y. Huang, C.-E. Wu, H.-M. Kao, RSC Adv. 6, 35167 (2016)

    Article  CAS  Google Scholar 

  13. X. Sheng, Y. Zhou, Y. Yang, Y. Zhang, Z. Zhang, S. Zhou, X. Fu, S. Zhao, RSC Adv. 4, 30697 (2014)

    Article  CAS  Google Scholar 

  14. S. Sadjadi, M.M. Heravi, Curr. Org. Chem. 20, 1404 (2016)

    Article  CAS  Google Scholar 

  15. J.J. Walsh, A.M. Bond, R.J. Forster, T.E. Keyes, Coord. Chem. Rev. 306, 217 (2016)

    Article  CAS  Google Scholar 

  16. L. Hong, Y. Gui, J. Lu, J. Hu, J. Yuan, L. Niu, Int. J. Hydrog. Energy 38, 11074 (2013)

    Article  CAS  Google Scholar 

  17. Y. Zhu, M. Zhu, L. Kang, F. Yu, B. Dai, Ind. Eng. Chem. Res. 54, 2040 (2015)

    Article  CAS  Google Scholar 

  18. J. Qu, Q. Zhang, X. Li, X. He, S. Song, Appl. Clay 119, 185 (2016)

    Article  CAS  Google Scholar 

  19. S. Omwoma, W. Chen, R. Tsunashima, Y.-F. Song, Coord. Chem. Rev. 258–259, 58 (2014)

    Article  Google Scholar 

  20. S.N. Basahel, S.A. Al-Thabaiti, K. Narasimharao, N.S. Ahmed, M. Mokhtar, J. Nanosci. Nanotechnol. 14, 1931 (2014)

    Article  CAS  Google Scholar 

  21. W. Guo, Y. Zhao, F. Zhou, X. Yan, B. Fan, R. Li, Appl. Catal. A 522, 101 (2016)

    Article  CAS  Google Scholar 

  22. T. Baskaran, J. Christopher, A. Sakthivel, RSC Adv. 5, 98853 (2015)

    Article  CAS  Google Scholar 

  23. D. Pan, H. Zhang, T. Fan, J. Chen, X. Duan, Chem. Commun. 47, 908 (2011)

    Article  CAS  Google Scholar 

  24. C.O. Kappe, Acc. Chem. Res. 33, 879 (2000)

    Article  CAS  Google Scholar 

  25. M.D. Burke, S.L. Schreiber, Angew. Chem. Int. Ed. 43, 46 (2004)

    Article  Google Scholar 

  26. J. Lu, P.H. Toy, Chem. Rev. 109, 815 (2009)

    Article  CAS  Google Scholar 

  27. A. Rahmati, Z. Khalesi, Tetrahedron 68, 8472 (2012)

    Article  CAS  Google Scholar 

  28. S.V.N. Vuppalapati, Y.R. Lee, Tetrahedron 68, 8286 (2012)

    Article  CAS  Google Scholar 

  29. C.-J. Li, T.-H. Chan, Comprehensive organic reactions in aqueous media (Wiley, New York, 2007)

    Book  Google Scholar 

  30. A. Chanda, V.V. Fokin, Chem. Rev. 109, 725 (2009)

    Article  CAS  Google Scholar 

  31. A. Schmidt, A. Dreger, Curr. Org. Chem. 15, 1423 (2011)

    Article  CAS  Google Scholar 

  32. A.N. Kost, I.I. Grandberg, Progress in pyrazole chemistry, in Advances in Heterocyclic Chemistry, vol. 6, ed. by A.R. Katritzky, A.J. Boulton (Academic Press, Cambridge, 1966), p. 347

    Google Scholar 

  33. W.S. Hamama, Synth. Commun. 31, 1335 (2001)

    Article  CAS  Google Scholar 

  34. W. Wang, S.X. Wang, X.Y. Qin, J.T. Li, Synth. Commun. 35, 1263 (2005)

    Article  CAS  Google Scholar 

  35. D. Singh, D. Singh, J. Chem. Eng. Data 29, 355 (1984)

    Article  CAS  Google Scholar 

  36. K. Niknam, D. Saberi, M. Sadegheyan, A. Deris, Tetrahedron Lett. 51, 692 (2010)

    Article  CAS  Google Scholar 

  37. D.Q. Shi, J. Chen, N. Wu, Q.Y. Zhuang, X.S. Wang, Chin. J. Org. Chem. 25, 405 (2005)

    CAS  Google Scholar 

  38. K. Sujatha, G. Shanthi, N.P. Selvam, S. Manoharan, P.T. Perumal, M. Rajendran, Bioorg. Med. Chem. Lett. 19, 4501 (2009)

    Article  CAS  Google Scholar 

  39. M.N. Nasr, M.M. Gineinah, Arch. Pharm. 335, 289 (2002)

    Article  CAS  Google Scholar 

  40. M.A. Zolfigol, M. Tavasoli, A.R. Moosavi-Zare, P. Moosavi, H.G. Kruger, M. Shiri, V. Khakyzadeh, RSC Adv. 3, 25681 (2013)

    Article  CAS  Google Scholar 

  41. V.K. Ahluwalia, A. Dahiya, V.K. Garg, Indian J. Chem. Sect. B. 36, 88 (1997)

    Google Scholar 

  42. N.R. Mohamed, N.Y. Khaireldin, A.F. Fahmy, A.A. El-Sayed, Der Pharma Chem. 2, 400 (2010)

    CAS  Google Scholar 

  43. H. Junek, H. Aigner, Chem. Ber. 106, 914 (1973)

    Article  CAS  Google Scholar 

  44. Y.A. Sharanin, L.G. Sharanina, V.V. Puzanova, Chem. Informationsdienst, 19, 2609–2615 (1983)

    CAS  Google Scholar 

  45. G. Vasuki, K. Kumaravel, Tetrahedron Lett. 49, 5636 (2008)

    Article  CAS  Google Scholar 

  46. M.M. Heravi, E. Hashemi, Y. Shirazi Beheshtiha, Sh Ahmadi, T. Hosseinnejad, J. Mol. Catal. A. 394, 74 (2014)

    Article  CAS  Google Scholar 

  47. M.M. Heravi, F. Mousavizadeh, N. Ghobadi, M. Tajbakhsh, Tetrahedron Lett. 55, 1226 (2014)

    Article  CAS  Google Scholar 

  48. S.S. Sadjadi, M.M. Heravi, V. Zadsirjan, V. Farzaneh, Appl. Surf. Sci. 426, 889 (2017)

    Article  Google Scholar 

  49. M. Hami Dindar, M.R. Yaftian, M. Hajihasani, S. Rostamnia, J. Taiwan Inst. Chem. Eng. 67, 325 (2016)

    Article  Google Scholar 

  50. A. Aouissi, Z.A. Al-Othman, H. Al-Anezi, Molecules 15, 3319 (2010)

    Article  CAS  Google Scholar 

  51. T. Baskaran, J. Christopher, T.G. Ajithkumar, A. Sakthivel, Appl. Catal. A. 488, 119 (2014)

    Article  CAS  Google Scholar 

  52. V. Fathi Vavsari, G. Mohammadi Ziarani, S. Balalaie, A. Latifi, M. Karimi, A. Badiei, Tetrahedron 72, 5420 (2016)

    Article  Google Scholar 

  53. S.K. Sharma, P.K. Kushwaha, V.K. Srivastava, S.D. Bhatt, R.V. Jasra, Ind. Eng. Chem. Res. 46, 4856 (2007)

    Article  CAS  Google Scholar 

  54. B. Wiyantoko, P. Kurniawati, T.E. Purbaningtias, I. Fatimah, Procedia Chem. 17, 21 (2015)

    Article  CAS  Google Scholar 

  55. Z. Wang, F. Liu, C. Lu, Chem. Commun. 47, 5479 (2011)

    Article  CAS  Google Scholar 

  56. S. Mallik, S.S. Dash, K.M. Parida, B.K. Mohapatra, J. Colloid Interface Sci. 300, 237 (2006)

    Article  CAS  Google Scholar 

  57. K.D. Parghi, J.R. Satam, R.V. Jayaram, Green Chem. Lett. Rev. 4, 143 (2011)

    Article  CAS  Google Scholar 

  58. K. Fan, J. Liu, X. Yang, L. Rong, RSC Adv. 5, 37916 (2015)

    Article  CAS  Google Scholar 

  59. Y. Peng, G. Song, R. Dou, Green Chem. 8, 573 (2006)

    Article  CAS  Google Scholar 

  60. M. Mirza-Aghayan, F. Saravani, A.A. Tarlani, M.S. Abaee, R. Boukherroub, Monatsh. Chem. 144, 1699 (2013)

    Article  CAS  Google Scholar 

  61. H. Sheibani, M. Babaie, Synth. Commun. 40, 257 (2009)

    Article  Google Scholar 

  62. J. Deng, L.-P. Mo, F.-Y. Zhao, Z.-H. Zhang, S.-X. Liu, ACS Comb. Sci. 14, 335 (2012)

    Article  CAS  Google Scholar 

  63. K. Kanagaraj, K. Pitchumani, Tetrahedron Lett. 51, 3312 (2010)

    Article  CAS  Google Scholar 

  64. A. Siddekha, A. Nizam, M.A. Pasha, Spectrochim. Acta Part A 81, 431 (2011)

    Article  CAS  Google Scholar 

  65. M.A.E.A.A. Ali, E. Remaily, S.K. Mohamed, Tetrahedron 70, 270 (2014)

    Article  Google Scholar 

  66. K. Ablajan, W. Liju, A. Tuoheti, Y. Kelimu, Lett. Org. Chem. 9, 639 (2012)

    Article  CAS  Google Scholar 

  67. M. Babaie, H. Sheibani, Arab. J. Chem. 4, 159 (2011)

    Article  CAS  Google Scholar 

  68. H. Mecadon, M.R. Rohman, M. Rajbangshi, B. Myrboh, Tetrahedron Lett. 52, 2523 (2011)

    Article  CAS  Google Scholar 

  69. R.-Y. Guo, Z.-M. An, L.-P. Mo, S.-T. Yang, H.-X. Liu, S.-X. Wang, Z.-H. Zhang, Tetrahedron 69, 9931 (2013)

    Article  CAS  Google Scholar 

  70. A. Vafaee, A. Davoodnia, M. Pordel, Res. Chem. Intermed. 41, 8343 (2015)

    Article  CAS  Google Scholar 

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Acknowledgements

The authors appreciate partial financial supports from Alzahra University and Iran Polymer and Petrochemical Institute. MMH is also thankful to the Iran National Science Foundation for the individual given grant.

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Correspondence to Samahe Sadjadi or Majid M. Heravi.

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Sadjadi, S., Heravi, M.M., Zadsirjan, V. et al. A ternary hybrid system based on combination of mesoporous silica, heteropolyacid and double-layered clay: an efficient catalyst for the synthesis of 2,4-dihydro-3H-pyrazol-3-ones and pyranopyrazoles in aqueous medium: studying the effect of the synthetic procedure on the catalytic activity. Res Chem Intermed 44, 6765–6785 (2018). https://doi.org/10.1007/s11164-018-3521-y

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