Synthesis And Identification Of from HEMA Schiff Base Derivatives Contains Aldehyde Group For Hexa and Hepta Cyclization

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Hamid Mohammed Saleh Al-Jubori

Abstract

In this research the polymer which contains aldehyde group [H1] has been prepared by oxidation [H] using the oxidizing agent (Dess Martin Periodinane), [H1] has been dialyzed by ethanol, Schiff bases[H2,H5andH8] compounds have been prepared through the reaction of compound [H1] with appropriate amines, [H3] compound which contains hydroquinazolin ring has been prepared by the reaction of [H2] compound with 2-amino benzoic acid.[H4]which has been prepared by cyclization reaction of compound [H2] with phthalic anhydride.  compounds [H6,H7]were prepared by the reaction of [H5] compound with 2-amino benzoic acid and phthalic acid anhydriede. Reaction of comp[H1] with 4-amino benzaldehyde afforded comp[8]. The [H9] compound prepared by the reaction of [H8] compound with thiocarbohydrazide, The structures of the synthesized compounds [1-9] have been characterized using avaible spectral ( IR, 1H-NMR) methods and the result obtained improved the structures assigned to these compounds

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Hamid Mohammed Saleh Al-Jubori. (2023). Synthesis And Identification Of from HEMA Schiff Base Derivatives Contains Aldehyde Group For Hexa and Hepta Cyclization. Tikrit Journal of Pure Science, 22(1), 83–94. https://doi.org/10.25130/tjps.v22i1.612
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References

1- Oyane A, Ishizone T, Uchida M, Furukawa K, Ushida T, Yokoyama H. Spontaneous formation of blood-compatible surfaces on hydrophobic polymers: surface enrichment of a block copolymer with a water-soluble block. Adv Mater (2005);17(19):2329–32.

2-Perrier, S.; P. Takolpuckdee. "Macromolecular Design via Reversible Addition–Fragmentation Chain Transfer (RAFT) / Xanthates (MADIX) Polymerization". J. Polym. Sci. Part A43(22): 53475393 Bibcode: (2005) Jpo SA. 43.5347 P. doi:

3-M. Atai, D.C. Watts, Z. Atai, Shrinkage strain-rates of dental resin- monomer and, composite systems, Biomaterials 26 (2005) 5015–50.

4 -L. Cianga, Y. Yagci, Synthesis and characterization of thiophene- substituted Nphenyl maleimide polymers by photoinduced radical polymerization, J. Polym. Sci. 40 (2002) 995–1004.

5-Kadriye,F,Hakan.J, Synthesis and characterization of conducting copolymers methyl ester of 3-thiophene acetic acid with pyrrole, J. Macromol. (2012).

6- A.A.H. Saeed, Indian J.Chem., 17B (1979)462.

7- R. M. Acheson, “An Introduction to Chemistry of Heterocyclic Compounds’’,(1976), 3rd Edn. 15.

8- J.B. Hendrickson, D. J. Cram and G. S. Hammond, “Organic Chemistry’’, 3rdEdn. Mc Grawn - Hill Inc. Japan,(1970), 967.

9- Chiefari, J.; Y.K. Chong, F. Ercole, J. Krstina, J. Jeffery, T.P.T. Le, R.T.A. Mayadunne, G.F. Meijs, C.L. Moad, G. Moad, E. Rizzardo, S.H. Thang ."Living Free-Radical Polymerization by Reversible Addition − Fragmentation Chain Transfer: The RAFT Process". Macromolecules 31 (16): 5559 – 5562. Bibcode: (1998) Ma Mol.. 31.5559C. doi: 10.1021/ ma 9804951

10-Han S, Hagiwara M, Ishizone T. Synthesis of thermally sensitive water-soluble polymethacrylates by living anionic polymerizations of oligo(ethylene glycol) methyl ether methacrylates. Macromolecules (2003); 36(22): 8312–9.

11- R.T. Morrison & R.N. Boyd, "Organic Chemistry". 8th Ed., Allyn & Bacon, Inc., USA (1984)741.

12- R.A.J. Al-Hassani, Ph.D. Thesis, Al-Nahrain University (2004) .

13- P. Stanetty, M.T urner & M.D. Mihovilovic, Molecules, 10 (2005) 367.

14- J.P. Henderikson , D.G. Gramm, G.S. Hamond, Translated by A.A. Yacine, G.H. Taman & M.A. Khahfa , "Organic Chemistry", 4th Ed. (1996)320.

15- Ch. J. Pouchert, "The Aldrich Library of NMR Spectra" 2nd Ed. (1983) 2 .