Synthesis of Some Arylidene Heterobicyclic Compounds using Nano Al2O3-SO3H under Sonication Conditions

Subject Areas : Polymer

Noshin Seif ¹ , Asadollah Farhadi ² , Rashid Badri ³ , Ali Reza Kiasat ⁴

1 - Department of Chemistry, Khuzestan Science and Research Branch, Islamic Azad University, Ahvaz, Iran. Department of Chemistry, Ahvaz Branch, Islamic Azad University, Ahvaz, Iran.
2 - Department of Chemistry, Ahvaz Branch, Islamic Azad University, Ahvaz, Iran. Petroleum University of Technology, Faculty of Science, Ahvaz, Iran.
3 - Department of Chemistry, Ahvaz Branch, Islamic Azad University, Ahvaz, Iran.
4 - Department of Chemistry, Ahvaz Branch, Islamic Azad University, Ahvaz, Iran. Chemistry Department, College of Science, Shahid Chamran University of Ahvaz, Ahvaz, Iran.

Received: 2021-11-21 Accepted : 2021-11-21 Published : 2021-10-01

Keywords: Nano Al2O3-SO3H, Arylidene heterobicyclic compounds, HCl (aq), Sonication ondition, Cyclopentanone,

References:

[1]. M. K. Mohammadi, S. J. Saghanezhad, N. Razzaghi-asl, Bull. Chem. Soc. Ethiop, 31,
535 (2017).
[2]. N. Nakamichi, Y. Kawashita, M. Hayashi, Synthesis, 1015 (2004).
[3]. K. S. Atwal, B. N. Swanson, S. E. Unger, D. M. Floyd, S. Moreland, A. Hedberg,
B.C. Oreilly, J. Med. Chem. 34, 806 (1991).
[4]. A. D. Patil, N. V. Kumar, W. C. Kokke, M. F. Bean, A. J. Freyer, C. D. Brosse, S.
Mai, A. Truneh, B. Carte, J. Org. Chem, 60, 1182 (1995).
[5]. H. I. EI-Subbagh, S. M. Abu-Zaid, M. A. Mahran, F. A. Badria, A. M. Al-Obaid, J.
Med. Chem, 43, 2915 (2000).

[6]. C. O. Kappe, Eur. J. Med. Chem, 35, 1043 (2000).
[7]. M. Ashok, B. S. Holla, N. S. Kumari, Eur. J. Med. Chem, 42, 380 (2007).
[8]. P. Biginelli, Gazz. Chim. Ital, 23, 360 (1893).
[9]. A. R. Hajipour, Y. Ghayeb, N. Sheikhan, A. E. Ruoho,Synth. Commun,41, 2226
(2011).
[10]. M. T. Maghsoodlou, R. Heydari,M. Lashkari, F. Mohamadpour, Indian J. Chem, 56B,
160 (2017).
[11]. A. Farhadi, M. A. Takassi, L. Hejazi, Z.Naturforsh, 68b, 51 (2013).
[12]. A. Farhadi, J. Noei, R. Haji Aliyari, M. Albakhtiyari, M. A. Takassi, Res. Chem.
Intermed, 42, 1401 (2015).
[13]. H. Kiyani, M. Ghiasi, J. Res. Chem. Intermed, 41,6635 (2015).
[14]. M. Ould M’hamed, A. G. Alshammari, O. M. Lemine, Appl. Sci, 6, 431 (2016).
[15]. Y. T. Reddy,R. P. Narsimha, B. S. Kumar, G. V. P. Rao, B. Rajitha,Indian J. Chem,
44B, 1304 (2005).
[16]. A. Farhadi, M. A. Takassi, L. Hejazi, Iran. Chem. Commun, 5, 35 (2017).
[17]. Y. L. Zhu, S. L. Huang, Y. J. Pan,Eur. J. Org. Chem, 11, 2354 (2005).
[18]. M. Mehrabi, A. Farhadi, A. R. Kiassat,Int. J. Org. Chem, 3, 240 (2017).
[19]. A. P. Martins. Marcos, P. Frizzo. Clarissa, N. Moreira. Dayse, L. Buriol, P. Machado,
Chem. Rev, 109, 4140 (2009).
[20]. T. J. Mason, L. Paniwnyk, J. P.Lorimer, Ultrason. Sonochem, 3, S253 (1996).
[21]. J. T. Li, J. F. Han, J. H. Yang, T. S.Li, Ultrason. Sonochem, 10, 119 (2003).
[22]. H. R. Memarian, A.Farhadi,Ultrason. Sonochem, 15, 1015 (2008).
[23]. H. R. Memarian, M. Soleymani, Ultrason. Sonochem, 18, 745 (2011).
[24]. M. Kalhor, Z. Zarnegar, RSC Adv, 9, 19333 (2019).
[25]. A. Bamoniri, N. Yaghmaeiyan-Mahabadi, Sci. Iran. C, 25, 1344 (2018).
[26]. L. Chen, J. Zhao, S. F. Yin, C. T. Au, RSC. Adv, 3, 3799 (2013).
[27]. A. Habibi, E. Ghanbari, I.Yavari, J. Iran. Chem. Soc. 16, 2519, (2019).
[28]. H. Faroughi Niya, N. Hazeri, M. T. Maghsoodlou, Appl. Organometal. Chem,
e5457, 1 (2020)

[29]. S. Sajjadifar, I. Amini, |G. Mansouri, S. Alimohammadi, Eurasian Chem. Commun.
2, 626 (2020).
[30]. A.Farhadi, M. A.Takassi, M.Enjilzadeh, F.Davod, J. Appl. Chem. Res, 12, 48
(2018).
[31]. A. R. Kiassat, S. Noorizadeh, M. Ghahremani, S. J. Saghanejad, J. Mol. Struc, 1036, 216-225 (((2013).
[32]. K. Aswin, M. Ghashang, S. S. Mansoor,Iran. J. Catal. 5, 175 (2015).
[33]. O. O. Ajani, R. I. Ituen, A. Falomo, Pak. J. Sci. Ind. Res. Ser. A: Phys. Sci, 54, 59
(2011).
[34]. A. Amoozadeh, S. Rahmani, F. Nemati, Heterocycl Commun, 19, 69 (2013).