[B(OH)3]0.78[B(OH)2(OSO3H)]0.22 as a new, cheap and eco-friendly catalyst for synthesis of acylals at room temperature under solvent free conditions
محورهای موضوعی : Iranian Journal of CatalysisBiBi Fatemeh Mirjalili 1 , Abdolhamid Bamoniri 2 , Fahimeh Kalantari 3
1 - Department of Chemistry, College of Science, Yazd University, P. O. Box 89195-741, Yazd. Iran.
2 - Department of Organic Chemistry, Faculty of Chemistry, University of Kashan, Kashan, Iran.
3 - Department of Chemistry, College of Science, Yazd University, P. O. Box 89195-741, Yazd. Iran.
کلید واژه: Aldehyde, Protecting group, [B(OH)3]0.78[B(OH)2(OSO3H)]0.22, Acylal, BSA,
چکیده مقاله :
[B(OH)3]0.78[B(OH)2(OSO3H)]0.22 or (BSA) was simply prepared by addition of chlorosulfonic acid to commercial boric acid at room temperature. This cheap and green solid acid was used as an efficient catalyst for synthesis of acylals from aldehydes under solvent-free conditions at room temperature.
[1] I. Lusticka, E. Vrbkova, E. Vyskocilova, I. Paterova, L. Cerveny, React. Kin. Mech. Catal. 108 (2013) 205-212.
[2] N.G. Khaligh, F. Shirini, Ultrason. Sonochem. 20 (2013) 19-25.
[3] G.M. Ziarani, A. Badiei, F. Shahjafari, T. Pourjafar, S. Afr. J. Chem. 65 (2012) 10-13.
[4] M. Yadegari, M. Moghadam, S. Tangestaninejad, V. Mirkhani, I. Mohammadpoor-Baltork, Inorg. Chim. Acta 388 (2012) 102-105.
[5] F. Shirini, O.G. Jolodar, J. Mol. Catal. A: Chem. 356 (2012) 61-69.
[6] F. Shirini, S. Akbari-Dadamahaleh, A. Mohammad-Khah, J. Mol. Catal. A: Chem. 363–364 (2012) 10-17.
[7] A.R. Massah, R.J. Kalbasi, A. Shafiei, Monatsh. Chem. 143 (2012) 643-652.
[8] Q. Liu, H.M. Ai, S. Feng, Synth. Commun. 42 (2012) 122-127.
[9] R.K. Kannasani, V.V. Satyanarayana Peruri, S.R. Battula, Chem. Cent. J. 6 (2012) 136-139.
[10] H.M. Al, Q. Liu, J. Chem. Soc. Pak. 34 (2012) 299-301.
[11] M.N. Sefat, A. Deris, K. Niknam, Chin. J. Chem. 29 (2011) 2361-2367.
[12] E. Saburi, A. Davoodnia, N. Tavakoli-Hoseini, Synth. React. Inorg. Metal-Org. Nano-Metal Chem. 41 (2011) 1063-1066.
[13] M.R. Nabid, S.J.T. Rezaei, M. Abedi, Synth. Commun. 41 (2011) 191-199.
[14] M. Moosavifar, S. Tangestaninejad, M. Moghadam, V. Mirkhani, I. Mohammadpoor-Baltork, C. R. Chim. 14 (2011) 953-956.
[15] C. Li, T. Guo, X. Zhou, C. Wang, J.J. Ma, J.B. Li, Lett. Org. Chem. 8 (2011) 484-487.
[16] A. Khazaei, A.A. Manesh, A. Rostami, H.A. Alavi-Nik, Z.T. Roosta, Asian J. Chem. 23 (2011) 614-616.
[17] A. Khazaei, A.A. Manesh, H.A. Alavi-Nik, Z.T. Roosta, Asian J. Chem. 23 (2011) 627-630.
[18] P. Gupta, S. Paul, Green Chem. 13 (2011) 2365-2372.
[19] K.P. Boroujeni, Synth. Commun. 41 (2011) 277-284.
[20] S.P. Borikar, T. Daniel, Ultrason. Sonochem. 18 (2011) 928-931.
[21] A. Bamoniri, A. Ghorbani-Choghamarani, B.F. Mirjalili, Phosphorus, Sulfur Silicon Relat. Elem. 186 (2011) 381-388.
[22] F.Y. Zhang, H. Liu, Q.J. Zhang, Y.F. Zhao, F.L. Yang, Synth. Commun. 40, (2010) 3240-3250.
[23] A. Zare, A. Hasaninejad, E. Rostami, A.R. Moosavi-Zare, M. Merajoddin, Sci. Iran. 17 (2010) 24-30.
[24] F. Shirini, M. Mamaghani, T. Mostashari-Rad, M. Abedini, Bull. Korean Chem. Soc. 31 (2010) 2399-2401.
[25] G.A. Meshram, V.D. Patil, Synth. Commun. 40 (2010) 442-449.
[26] Y.Q. Zhang, M.Y. Zhang, W.H. Liu, Y.M. Li, M. Liu, C. Wang, Chin. J. Org. Chem. 29 (2009) 1259-1263.
[27] A. Zare, A. Hasaninejad, E. Rostami, A.R. Moosavi-Zare, M. Merajoddin, A. Arghoon, N. Pishahang, M. Shekouhy, E-J. Chem. 6 (2009) S390-S396.
[28] B.F. Mirjalili, M.A. Zolfigol, A. Bamoniri, M.A. Amrollahi, N. Sheikhan, Russ. J. Org. Chem. 43 (2007) 852-854.
[29] M. Wang, G.F. Tian, Z.G. Song, H. Jiang, Chin. Chem. Lett. 20 (2009) 1034-1038.
[30] N. Sheikhan, B.F. Mirjalili, A. Hajipour, A. Bamoniri, Acta Chim. Sloven. 55 (2008) 209-218.
[31] J.R. Satam, R.V. Jayaram, Catal. Commun. 8 (2007) 1414-1420.
[32] A.R. Hajipour, A. Zarei, L. Khazdooz, B.B.F. Mirjalili, N. Sheikhan, S. Zahmatkesh, A.E. Ruoho, Synthesis (2005) 3644-3648.
[33] B.F. Mirjalili, M.A. Zolfigol, A. Bamoniri, N. Sheikhan, J. Chin. Chem. Soc. 53 (2006) 955-959.
[34] R. Kumar, P. Tiwari, P.R. Maulik, A.K. Misra, J. Mol. Catal. A: Chem. 247 (2006) 27-30.
[35] K. Niknam, D. Saberi, M.N. Sefat, Tetrahedron Lett. 50 (2009) 4058-4062.
[36] A. R. Kiasat, M. Fallah-Mehrjardi, J. Braz. Chem. Soc. 19 (2008) 1595-1599.
