Nano-BF3/cellulose as a biodegradable novel catalyst for synthesis of highly functionalized tetrahydropyridines
الموضوعات : Iranian Journal of Catalysis
Seyede Azita Fazeli-Attar
1
(Department of Chemistry, College of Science, Yazd University, Yazd, P.O. Box. 89195-741, I. R. Iran.)
Bi Bi Fatemeh Mirjalili
2
(Department of Chemistry, College of Science, Yazd University, Yazd, P.O. Box. 89195-741, I. R. Iran.)
الکلمات المفتاحية: Multicomponent reactions, Solid acid, Tetrahydropyridines, Nano-BF3/cellulose,
ملخص المقالة :
Nano-cellulose with high amount of free OH groups could be used as supporting agents for boron trifluoride (BF3). Nano-BF3/cellulose is a solid acid and a biodegradable catalyst which was prepared via reaction of nano-cellulose and BF3. The structure of this catalyst was studied by FT-IR, FESEM, TEM, XRD, EDS, TGA, XRF and BET. In this research, the synthesis of highly functionalized tetrahydropyridines has been developed via a five-component reaction of aldehyde, amine and ethyl acetoacetate using nano-BF3/cellulose under solvent-free conditions. The structures of obtained products were identified by FTIR, 1H NMR and 13C NMR. Some advantages of this protocol are high to good yields, environmentally benign procedure, easy work-up of reaction and moderate reusability of the catalyst.
[1] L. Constantino, D. Barlocco, Curr. Med. Chem. 13 (2008) 65-85.
[2] A. Zare, E. Sharif, A. Arghoon, M. Ghasemi, B. Dehghani, S. Ahmad-Zadeh, F. Zarei, Iran. J. Catal. 7 (2017) 233-241.
[3] R. Magar, G. Pawar, S. Gadekar, M. Lande, Iran. J. Catal. 7 (2017) 1-9.
[4] R. Singh, S. Sharma, A. Sandhar, M. Saini, S. Kumar, Iran. J. Catal. 6 (2016) 1-21.
[5] R. Singh, R. Bala, R. Duvedi, S. Kumar, Iran. J. Catal. 5 (2015) 187-206.
[6] M. Misra, S.K. Pandey, V.P. Pandey, J. Pandey, R. Tripathi, R.P. Tripathi, Bioorg. Med. Chem. 17 (2009) 625-633.
[7] R. Aeluri, M. Alla, V.R. Bommena, R. Murthy, N. Jain, Asian J. Org. Chem. 1 (2012) 71-79.
[8] J. Stephen, M.D. Peroutka, H. Solomon, M.D. Snyder, Am. J. Psych. 137 (1980) 1518-1522.
[9] A.D. Korczyn, Expert Opin. Investig. Drugs 9 (2000) 2259-2267.
[10] H. Kitagawa, T. Takenouchi, R. Azuma, K.A. Wesnes, W.G. Kramer, D.E. Clody, A.L. Burnett, Neuropsychopharmacology 28 (2003) 542-551.
[11] M.D. Mashkovskii, R.G. Glushkov, Pharm. Chem. J. 35 (2001) 179-182.
[12] A.T. Khan, T. Parvin, L.H. Choudhury, J. Org. Chem. 73 (2008) 8398-8402.
[13] T. Khan, M. Lal, M.M. Khan, Tetrahedron Lett. 51 (2010) 4419-4424.
[14] T. Khan, M.M. Khan, K.K.R. Bannuru, Tetrahedron 66 (2010) 7762-7772.
[15] H.J. Wang, L.P. Mo, Z.H. Zhang, ACS Comb. Sci.13 (2011) 181-185.
[16] S. Mishra, R. Ghosh, Tetrahedron Lett. 52 (2011) 2857-2861.
[17] S.S. Sajadikhah, M.T. Maghsoodlou, N. Hazeri, S.M. Habibi-Khorassani, S.J. Shams-Najafi, Monatsh Chem. 143 (2012) 939-945.
[18] N. Hazeri, M.T. Maghsoodlou, S.M. Habibi‐Khorassani, J. Aboonajmi, S.S. Sajadikhah, J. Chin. Chem. Soc. 60 (2013) 355-358.
[19] J. Safaei-Ghomi, A. Ziarati, J. Iran. Chem. Soc. 10 (2013) 135-139.
[20] M. Lashkari, M.T. Maghsoodlou, N. Hazeri, S.M. Habibi-Khorassani, S.S. Sajadikhah, R. Doostmohamadi, Synth. Commun. 43 (2013) 635-644.
[21] R. Ramachandran, S. Jayanthi, Y.T. Jeong, Tetrahedron 68 (2012) 363-369.
[22] G. Harichandran, S.D. Amalraj, P. Shanmugam, J. Heterocyclic Chem. 50 (2013) 539-543.
[23] H. Eshghi, A. Khojastehnezhad, F. Moeinpour, M. Bakavoli, S.M. Seyedi, M. Abbasi, RSC Adv. 4 (2014) 39782-39789.
[24] N.R. Agrawal, S.P. Bahekar, P.B. Sarode, S.S. Zade, H.S. Chandak, RSC Adv. 5 (2015) 47053-47059.
[25] M. Daraei, M.A. Zolfigol, F. Derakhshan-Panah, M. Shiri, H.G. Kruger, M. Mokhlesi, J. Iran. Chem. Soc. 12 (2015) 855-861.
[26] M. Kataria, S. Pramanik, M. Kumar, V. Bhalla, Chem. Commun. 51 (2015) 1483-1486.
[27] M. Abbasi, S.M. Seyedi, H. Sadeghian, M. Akhbari, M. Enayaty, A. Shiri, Heterocycl. Commun. 22 (2016) 117-121.
[28] M. Maghsoodlou, N. Hazeri, E. Fereidooni, S. Salahi, N. Mahmoudabadi, N. Khorshidi, J. Aboonajmi, M. Lashakri, Iran. J. Catal. 5 (2015) 245-252.
[29] Z. Benzekribe, H. Serrar, A. Zarguil, S. Boukhris, A. Souizi, Iran. J. Catal. 8 (2018) 1-7.
[30] S.C. Azimi, H. Kefayati, Iran. J. Catal. 3 (2013) 123-128.
[31] K.F. Shelke, S.B. Sapkal, G.K. Kakade, B.B. Shingate, M.S. Shingare, Green Chem. Lett. Rev. 3 (2010) 27-32.
[32] J. Safari, S.H. Banitaba, S.D. Khalili, J. Mol. Catal A: Chem. 335 (2011) 46-50.
[33] S. Azad, B.F. Mirjalili, RSC Adv. 6 (2016) 96928-96934.
[34] C. Mukhopadhyay, S. Rana, R.J. Butcher, A.M. Schmiedekamp, Tetrahedron Lett. 52 (2011) 5835-5840.
[35] E. Babaei, B. F. Mirjalili, Res. Chem. Intermed. 44 (2018) 3493–3505.
