CiteScore: 1.8     h-index: 21

Document Type : Original Research Article


1 Department of Chemistry, Payame Noor University, Tehran, P.O. Box 19395-4697, Iran

2 Research Center of Environmental Chemistry, Payame Noor University, Ardakan, Yazd, Iran


1-amidoalkyl-2-naphthols were prepared via one-pot multi-component reaction of 2-naphthol, aldehydes, and amides in the presence of nickel nanoparticles as a solid phase acidic catalyst, under solvent-free condition at 100 °C. The recent literature survey reveals that the nano nickel was used as heterogeneous catalyst and received noteworthy attention because of its inexpensive, non-toxic, low corrosion, waste minimization, easy transport and disposal of the catalyst. Short reaction times, high yields, and easy work-up are the advantages of this protocol.

Graphical Abstract

A new application of nickel nanoparticles as a heterogeneous catalyst for synthesis of 1-amidoalkyl-2-naphthols according to green chemistry principles


Main Subjects

[2]. Dallinger D., Stadler A., Kappe C.O. Pure Appl. Chem., 2004, 76:1017
[3]. Ugi I., Werner B., Domling A. Molecules, 2003, 8:53
[4]. Trost B.M. Acc. Chem. Res., 2002, 35:695
[5]. Mullin R. Chem. Eng. News, 2004, 82:29
[6]. Wang Y.F., Lzawa T., Kobayashi S., Ohno M. J. Am. Chem. Soc., 1982, 104:6456
[7]. Shen A.Y., Tsai C.T., Chen C.L. Eur. J. Chem., 1997, 34:877
[8]. Cai X.H., Guo H., Xie B. Int. J. Chem., 2011, 3:119
[10]. Zolfigol M.A., Khazaei A., Moosavi-Zare A.R., Zare A., Khakyzadeh V. Appl. Catal. A: Gen., 2011, 400:70
[11]. Khazaei A., Zolfigol M.A., Moosavi-Zare A.R., Abi F., Zare A., Kaveh H., Khakyzadeh V., Kazem-Rostami M., Parhami A., Torabi-Monfared H. Tetrahedron, 2013, 69:212
[12]. Zare A., Yousofi T., Moosavi-Zare A.R. RSC Adv., 2012, 2:7988
[13]. Zare A., Hasaninejad A., Rostami E., Moosavi-Zare A.R., Pishahang N., Roshankar M., Khedri M. E. J. Chem., 2010, 7:1162
[14]. Hajipour A.R., Ghayeb Y., Sheikhan N., Ruoho A.E. Tetrahedron Lett., 2009, 50:5649
[15]. Supale A.R., Gokavi G.S. J. Chem. Sci., 2010, 122:189
[16]. Zhang Q., Luo J., Wei Y. Green Chem., 2010, 12:2247
[17]. Hakimi F. J. Chem. Res., 2016, 40:489
[18]. Hakimi F. Synth. React. Inorg. M., 2017, 47:994
[19]. Mirkin C.A., Letsinger R.L., Mucic R.C., Storhoff J.J. Nature, 1996, 382:607
[20]. Storhoff J.J., Elghanian R., Mucic R.C., Mirkin C.A., Letsinger R.L. J. Am. Chem. Soc., 1998, 120:1959
[21]. Morozov Y.G., Belousova O.V., Kuznetsov M.V. Inorg. Mater., 2011, 47:36
[22]. Saxena A., Kumar A., Mozumdar S. J. Mol. Catal. A: Chem., 2007, 269:35
[23]. Khurana J.M., Vij K. J. Chem. Sci., 2012, 124:907
[24]. Jiang Z., Xie J., Jiang D., Wei X., Chen M. Cryst. Eng. Comm., 2013, 15:560
[25]. Sapkal S., Shelke K., Shingate B., Shingare M. Tetrahedron Lett., 2009, 50:1754
[26]. Banitaba S.H., Dehghan Khalili S., Safari J. Iran J. Org. Chem., 2012, 4:785
[27]. Olyaei A., Vaziri M., Razeghi R., Shams B., Bagheri H. J. Serb. Chem. Soc., 2013, 78:463
[28]. Dhakshinamoorthy A., Pitchumani K. Tetrahedron Lett., 2008, 49:1818
[29]. Chou K., Huang K. J. Nanopart. Res., 2001, 3:127
[30]. Luo J., Zhang Q. Monatsh Chem., 2011, 141:923
[31]. Mirjalili B.F., Bamoniri A., Rahmati L. Arabian J. Chem., 2014, 11:653
[32]. Habibzadeh S., Ghasemnejad H. J. Chin. Chem. Soc., 2012, 59:193
[33]. Shaterian H.R., Yarahmadi H., Ghashang M. Bioorg. Med. Chem. Lett., 2008, 18:788
[34]. Patil S.B., Singh P.R., Surpur M.P., Samant S.D. Ultrason. Sonochem., 2007, 14:515