Generic placeholder image

Letters in Organic Chemistry

Editor-in-Chief

ISSN (Print): 1570-1786
ISSN (Online): 1875-6255

Research Article

Synthesis of Amidoalkyl Naphthols in PEG-400 as a Green and Efficient Solvent and Theoretical Study of their Spectroscopic Properties

Author(s): Marjan Rezaeipour, Ahmad Momeni Tikdari, Hojatollah Khabazzadeh* and Vahid Saheb

Volume 19, Issue 2, 2022

Published on: 10 June, 2021

Page: [150 - 157] Pages: 8

DOI: 10.2174/1570178618666210610170234

Price: $65

Abstract

An efficient synthesis of amidoalkyl naphthols from the multicomponent reaction of 2- naphthol, aromatic aldehydes, and benzamide derivatives using PEG-400 as an environmentally friendly solvent is described. The main advantage of this protocol is that the benzamide derivatives with low reactivity, such as 4-nitro benzamide, can react effectively.

Also, the molecular structure, IR, and 13C NMR spectra of the synthesized compounds are also investigated theoretically. Density functional theory (DFT) calculations at the B3LYP level of theory are carried out to locate optimized geometries and calculate vibrational normal modes and 13C NMR chemical shifts. These calculations enable us to assign the observed FT-IR and 13C NMR peaks to the corresponding vibrational motions and 13C atoms, respectively.

Keywords: Amidoalkyl naphthol, PEG-400, green, 4-substituted benzamide, 2-Naphthol, DFT.

Graphical Abstract

[1]
Kusakabe, Y.; Nagatsu, Y.; Shibuya, J.; Kawaguchi, M.; Hirose, O.; Shirato, C.S. J. Antibiot., 1972, 25, 44.
[http://dx.doi.org/10.7164/antibiotics.25.44]
[2]
Ren, H.; Grady, S.; Gamenara, D.; Heinzen, H.; Moyna, P.; Croft, S.L.; Kendrick, H.; Yardley, V.; Moyna, G. Bioorg. Med. Chem. Lett., 2001, 11(14), 1851-1854.
[http://dx.doi.org/10.1016/S0960-894X(01)00308-0] [PMID: 11459645]
[3]
Peglion, J.L.; Vian, J.; Gourment, B.; Despaux, N.; Audiont, V.; Millan, M. Bioorg. Med. Chem. Lett., 1997, 7, 881.
[http://dx.doi.org/10.1016/S0960-894X(97)00126-1]
[4]
Darbandi, H.; Kiyani, H. Curr. Organocatal., 2020, 7, 34.
[http://dx.doi.org/10.2174/2213337206666190515091358]
[5]
Kantevari, S.; Vuppalapati, S.V.N.; Nagarapu, L. Catal. Commun., 2007, 8, 1857.
[http://dx.doi.org/10.1016/j.catcom.2007.02.022]
[6]
Torabi, M.; Yarie, M.; Zolfigol, M.A.; Azizian, S. Res. Chem. Intermed., 2020, 46, 891.
[http://dx.doi.org/10.1007/s11164-019-03996-w]
[7]
Hashemi, H.; Sardarian, A.R.J. Iran. Chem. Soc., 2013, 10, 745.
[http://dx.doi.org/10.1007/s13738-012-0208-y]
[8]
Istran, T.H.; Paul, A. Chem. Rev., 2007, 107, 2169.
[http://dx.doi.org/10.1021/cr078380v] [PMID: 17564478]
[9]
Prat, D.; Pardigon, O.; Flemming, H.W.; Letestu, S.; Ducandas, V.; Isnard, P.; Guntrum, E.; Senac, T.; Ruisseau, S.; Cruciani, P.; Hosek, P. Org. Process Res. Dev., 2013, 17, 1517.
[http://dx.doi.org/10.1021/op4002565]
[10]
Taghrir, H.; Ghashang, M.; Biregan, M.N. Chin. Chem. Lett., 2016, 27, 119.
[http://dx.doi.org/10.1016/j.cclet.2015.08.011]
[11]
Tamaddon, F.; Moazeni Bistgani, J. Synlett, 2011, 2947.
[http://dx.doi.org/10.1055/s-0031-1289906]
[12]
Mou, J.; Gao, G.; Chen, C.; Liu, J.; Gao, J.; Liu, Y. RSC Advances, 2017, 7, 13868.
[http://dx.doi.org/10.1039/C6RA28599F]
[13]
Becke, A.D. J. Chem. Phys., 1993, 98, 5648.
[http://dx.doi.org/10.1063/1.464913]
[14]
Lee, C.; Yang, W.; Parr, R.G. Phys. Rev. B Condens. Matter, 1988, 37(2), 785-789.
[http://dx.doi.org/10.1103/PhysRevB.37.785] [PMID: 9944570]
[15]
Sheik Mansoor, S.; Aswin, K.; Logaiya, K.; Sudhan, S.P.N. J. Saudi Chem. Soc., 2016, 20, 138.
[http://dx.doi.org/10.1016/j.jscs.2012.06.003]
[16]
Shaterian, H.R.; Azizi, K.; Fahimi, N. Chem. Sci. Trans., 2012, 1, 73.
[http://dx.doi.org/10.7598/cst2012.139]
[17]
Alecu, I.M.; Zheng, J.; Zhao, Y.; Truhlar, D.G. J. Chem. Theory Comput., 2010, 6(9), 2872-2887.
[http://dx.doi.org/10.1021/ct100326h] [PMID: 26616087]
[18]
Sheikhshoaie, I.; Saheb, V. Spectrochim. Acta A Mol. Biomol. Spectrosc., 2010, 77(5), 1069-1076.
[http://dx.doi.org/10.1016/j.saa.2010.08.075] [PMID: 20889369]
[19]
Bazgir, A.; Amani, V.; Khavasi, H.R. Acta Crystallogr., 2006, E62, o5523.
[20]
Wolinski, K.; Hilton, J.F.; Pulay, P. J. Am. Chem. Soc., 1990, 112, 8251.
[http://dx.doi.org/10.1021/ja00179a005]
[21]
Cossi, M.; Rega, N.; Scalmani, G.; Barone, V. J. Comput. Chem., 2003, 24(6), 669-681.
[http://dx.doi.org/10.1002/jcc.10189] [PMID: 12666158]
[22]
Frisch, M.J.; Trucks, G.W.; Schlegel, H.B.; Scuseria, G.E.; Robb, M.A.; Cheeseman, J.R.; Scalmani, G.; Barone, V.; Mennucci, B.; Petersson, G.A.; Nakatsuji, H.; Caricato, M.; Li, X.; Hratchian, H.P.; Izmaylov, A.F.; Bloino, J.; Zheng, G.; Sonnenberg, J.L.; Hada, M.; Ehara, M.; Toyota, K.; Fukuda, R.; Hasegawa, J.; Ishida, M.; Nakajima, T.; Honda, Y.; Kitao, O.; Nakai, H.; Vreven, T.; Montgomery, J.A.; Peralta, J.E.; Ogliaro, F.; Bearpark, M.; Heyd, J.J.; Brothers, E.; Kudin, K.N.; Staroverov, V.N.; Kobayashi, R.; Normand, J.; Raghavachari, K. Rendell, A.; Burant, J. C.; Iyengar, S. S.; Tomasi, J.; Cossi, M.; Rega, N.; Millam, J. M.; Klene, M.; Knox, J. E.; Cross, J. B.; Bakken, V.; Adamo, C.; Jaramillo, J.; Gomperts, R.; Stratmann, R. E.; Yazyev, O.; Austin, A. J.; Cammi, R.; Pomelli, C.; Ochterski, J. W.; Martin, R. L.; Morokuma, K.; Zakrzewski, V. G.; Voth, G. A.; Salvador, P.; Dannenberg, J. J.; Dapprich, S.; Daniels, A. D.; Farkas, O.; Foresman, J. B.; Ortiz, J. V.; Cioslowski, J.; Fox, D. J. Gaussian 09, Revision A.1; Gaussian, Inc.: Wallingford, CT, 2009.

Rights & Permissions Print Cite
© 2024 Bentham Science Publishers | Privacy Policy