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One Pot Synthesis and Characterization of Mono and Di-Substituted Azo-Containing Amides
Corresponding Author(s) : Rasheed Ahmad Khera
Asian Journal of Chemistry,
Vol. 27 No. 6 (2015): Vol 27 Issue 6
Abstract
Azo-containing amides and their derivatives were synthesized by the reaction of 4-(phenyldiazenyl)aniline with different substituted benzoyl chlorides. The characterization of these synthesized compounds were based on their IR, 1H NMR spectra and elemental analysis with excellent yields.
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- J.M. Humphrey and A.R. Chamberlin, Chem. Rev., 97, 2243 (1997); doi:10.1021/cr950005s.
- K. Ekoue-Kovi and C. Wolf, Chem. Eur. J., 14, 6302 (2008); doi:10.1002/chem.200800353.
- D. Döpp and H. Döpp, Houben-Weyl, Methoden der organischen Chemie, Thieme, Stuttgart, vol. E5, pp. 934 (1985).
- R.C. Larock, Comprehensive Organic Transformations: A Guide to Functional Group Preparations, VCH, Weinheim (1989).
- H.U. Vora and T. Rovis, J. Am. Chem. Soc., 129, 13796 (2007); doi:10.1021/ja0764052.
- L. Zhang, S. Wang, S. Zhou, G. Yang and E. Sheng, J. Org. Chem., 71, 3149 (2006); doi:10.1021/jo060063l.
- P.M. Miladinova and T.N. Konstantinova, Color. Technol., 125, 242 (2009); doi:10.1111/j.1478-4408.2009.00203.x.
- H. Zollinger, Azo and Diazo Chemistry, Interscience, New York (1961).
- H. Zollinger, Colour Chemistry, Syntheses, Properties, and Applications of Organic Dyes, Weinheim: VCH (1987).
- K. Singh, S. Singh, A. Mahajan and J.A. Taylor, Color Technol., 119, 198 (2003); doi:10.1111/j.1478-4408.2003.tb00172.x.
- H.S. Bhatti and S. Seshadri, Color Technol., 120, 151 (2004); doi:10.1111/j.1478-4408.2004.tb00221.x.
- R.H. El Halabieh, O. Mermut and C.J. Barrett, J. Pure Appl. Chem., 76, 1445 (2004); doi:10.1351/pac200476071445.
- I. Sener and F. Kadifeli, Color Technol., 127, 404 (2011); doi:10.1111/j.1478-4408.2011.00337.x.
- H. Nishihara, Bull. Chem. Soc. Jpn., 77, 407 (2004); doi:10.1246/bcsj.77.407.
- L. He, L. Lu, S. Zhang and H.S. Freeman, Color. Technol., 126, 92 (2010); doi:10.1111/j.1478-4408.2010.00232.x.
- K.R. Naqvi and M. Clark, Color Technol., 127, 62 (2011); doi:10.1111/j.1478-4408.2010.00279.x.
- A.F. Little and R.M. Christie, Color Technol., 127, 275 (2011); doi:10.1111/j.1478-4408.2011.00307.x.
- V.S. Palekar, N.D. Pingale and S.R. Shukla, Color Technol., 126, 86 (2010); doi:10.1111/j.1478-4408.2010.00231.x.
- E. Hamada, T. Fujii, Y. Tomizawa and S. Iimura, Jpn. J. Appl. Phys., 36(Part 1, No. 1B), 593 (1997); doi:10.1143/JJAP.36.593.
- Y. Suzuki, Y. Okamoto, Y. Kurose and S. Maeda, Jpn. J. Appl. Phys., 38(Part 1, No. 3B), 1669 (1999); doi:10.1143/JJAP.38.1669.
- H. Nakazumi, E. Hamada, T. Ishiguro, H. Shiozaki and T. Kitao, J. Soc. Dyers Colour, 105, 1989 (1986).
- A.A. Khandar and Z. Rezvani, Polyhedron, 18, 129 (1998); doi:10.1016/S0277-5387(98)00275-7.
- J.H. Choi, O.T. Kwon, H.Y. Lee, A.D. Towns and C. Yoon, Color Technol., 126, 237 (2010); doi:10.1111/j.1478-4408.2010.00252.x.
- P.P. Kasture, Y.A. Sonawane, R.N. Rajule and G.S. Shankarling, Color Technol., 126, 348 (2010); doi:10.1111/j.1478-4408.2010.00268.x.
- A.A. Khandar, Z. Rezvani, K. Nejati, A.I. Yanovsky and J.M. Martinez, Acta Chim. Slov., 49, 733 (2002).
- Z. Rezvani, A.R. Abbasi, K. Nejati and M. Seyedahmadian, Polyhedron, 24, 1461 (2005); doi:10.1016/j.poly.2005.03.096.
- Z. Rezvani, L. Rahimi Ahar, K. Nejati and S.M. Seyedahmadian, Acta Chim. Slov., 51, 675 (2004).
- A.R. Abbasi, Z. Rezvani and K. Nejati, Dyes Pigments, 70, 71 (2006); doi:10.1016/j.dyepig.2005.04.015.
- Z. Rezvani, B. Divband, A.R. Abbasi and K. Nejati, Polyhedron, 25, 1915 (2006); doi:10.1016/j.poly.2005.12.016.
- J. Hooker, D. Hinks, G. Montero and C. Conlee, Color Technol, 118, 273 (2002); doi:10.1111/j.1478-4408.2002.tb00110.x.
- A. Saeed, R.A. Khera and M. Parvez, Acta Crystallogr., 66E, 635 (2010); doi:10.1107/S1600536810004708.
- A. Saeed, R.A. Khera, M. Siddiq and J. Simpson, Acta Crystallogr., 66E, 19 (2010); doi:10.1107/S1600536809050946.
References
J.M. Humphrey and A.R. Chamberlin, Chem. Rev., 97, 2243 (1997); doi:10.1021/cr950005s.
K. Ekoue-Kovi and C. Wolf, Chem. Eur. J., 14, 6302 (2008); doi:10.1002/chem.200800353.
D. Döpp and H. Döpp, Houben-Weyl, Methoden der organischen Chemie, Thieme, Stuttgart, vol. E5, pp. 934 (1985).
R.C. Larock, Comprehensive Organic Transformations: A Guide to Functional Group Preparations, VCH, Weinheim (1989).
H.U. Vora and T. Rovis, J. Am. Chem. Soc., 129, 13796 (2007); doi:10.1021/ja0764052.
L. Zhang, S. Wang, S. Zhou, G. Yang and E. Sheng, J. Org. Chem., 71, 3149 (2006); doi:10.1021/jo060063l.
P.M. Miladinova and T.N. Konstantinova, Color. Technol., 125, 242 (2009); doi:10.1111/j.1478-4408.2009.00203.x.
H. Zollinger, Azo and Diazo Chemistry, Interscience, New York (1961).
H. Zollinger, Colour Chemistry, Syntheses, Properties, and Applications of Organic Dyes, Weinheim: VCH (1987).
K. Singh, S. Singh, A. Mahajan and J.A. Taylor, Color Technol., 119, 198 (2003); doi:10.1111/j.1478-4408.2003.tb00172.x.
H.S. Bhatti and S. Seshadri, Color Technol., 120, 151 (2004); doi:10.1111/j.1478-4408.2004.tb00221.x.
R.H. El Halabieh, O. Mermut and C.J. Barrett, J. Pure Appl. Chem., 76, 1445 (2004); doi:10.1351/pac200476071445.
I. Sener and F. Kadifeli, Color Technol., 127, 404 (2011); doi:10.1111/j.1478-4408.2011.00337.x.
H. Nishihara, Bull. Chem. Soc. Jpn., 77, 407 (2004); doi:10.1246/bcsj.77.407.
L. He, L. Lu, S. Zhang and H.S. Freeman, Color. Technol., 126, 92 (2010); doi:10.1111/j.1478-4408.2010.00232.x.
K.R. Naqvi and M. Clark, Color Technol., 127, 62 (2011); doi:10.1111/j.1478-4408.2010.00279.x.
A.F. Little and R.M. Christie, Color Technol., 127, 275 (2011); doi:10.1111/j.1478-4408.2011.00307.x.
V.S. Palekar, N.D. Pingale and S.R. Shukla, Color Technol., 126, 86 (2010); doi:10.1111/j.1478-4408.2010.00231.x.
E. Hamada, T. Fujii, Y. Tomizawa and S. Iimura, Jpn. J. Appl. Phys., 36(Part 1, No. 1B), 593 (1997); doi:10.1143/JJAP.36.593.
Y. Suzuki, Y. Okamoto, Y. Kurose and S. Maeda, Jpn. J. Appl. Phys., 38(Part 1, No. 3B), 1669 (1999); doi:10.1143/JJAP.38.1669.
H. Nakazumi, E. Hamada, T. Ishiguro, H. Shiozaki and T. Kitao, J. Soc. Dyers Colour, 105, 1989 (1986).
A.A. Khandar and Z. Rezvani, Polyhedron, 18, 129 (1998); doi:10.1016/S0277-5387(98)00275-7.
J.H. Choi, O.T. Kwon, H.Y. Lee, A.D. Towns and C. Yoon, Color Technol., 126, 237 (2010); doi:10.1111/j.1478-4408.2010.00252.x.
P.P. Kasture, Y.A. Sonawane, R.N. Rajule and G.S. Shankarling, Color Technol., 126, 348 (2010); doi:10.1111/j.1478-4408.2010.00268.x.
A.A. Khandar, Z. Rezvani, K. Nejati, A.I. Yanovsky and J.M. Martinez, Acta Chim. Slov., 49, 733 (2002).
Z. Rezvani, A.R. Abbasi, K. Nejati and M. Seyedahmadian, Polyhedron, 24, 1461 (2005); doi:10.1016/j.poly.2005.03.096.
Z. Rezvani, L. Rahimi Ahar, K. Nejati and S.M. Seyedahmadian, Acta Chim. Slov., 51, 675 (2004).
A.R. Abbasi, Z. Rezvani and K. Nejati, Dyes Pigments, 70, 71 (2006); doi:10.1016/j.dyepig.2005.04.015.
Z. Rezvani, B. Divband, A.R. Abbasi and K. Nejati, Polyhedron, 25, 1915 (2006); doi:10.1016/j.poly.2005.12.016.
J. Hooker, D. Hinks, G. Montero and C. Conlee, Color Technol, 118, 273 (2002); doi:10.1111/j.1478-4408.2002.tb00110.x.
A. Saeed, R.A. Khera and M. Parvez, Acta Crystallogr., 66E, 635 (2010); doi:10.1107/S1600536810004708.
A. Saeed, R.A. Khera, M. Siddiq and J. Simpson, Acta Crystallogr., 66E, 19 (2010); doi:10.1107/S1600536809050946.