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Acetalization Of Carbonyl Compounds By Using Al2 (Hpo4)3 Under Green Condition Mg Hpo4

Authors: Jafari, Fariba; Samaneh Heydarian;

Acetalization Of Carbonyl Compounds By Using Al2 (Hpo4)3 Under Green Condition Mg Hpo4

Abstract

{"references": ["B. Karimi, A. Ashtiani, \"Chem. Lett\", vol. 28, 1999, pp. 1199.", "B. Karimi, H. Seradj, G. R. Ebrahimian, \"Syn. Let. 1999\", pp. 1456.", "A. Corma, C. Opin, \"Solid State Mat. Sci\", vol 2, 1997, pp. 63.", "S. K. Sikdar, S. G. Howell, \"J. Cleaner Production\", vol. 6, 1998, pp.\n253.", "R. Gopinath, S. J. Haque, B. K. Patel, \"J. Org. Chem\", vol. 67 2002, pp.\n5842.", "S. J. Ji, L. Wu, \"J. Mol. Catal. A. Chem\", vol. 41, 2003, pp. 202.", "W. B. Wang, L. L. Shi, Y. Z. Huang, \"Tetrahedron\", vol. 46, 1990, pp.\n3315.", "J. S. Yadav, B. V. Subba Reddy, R. Srinivas, T. Ramalingam, \"Syn.\nLett\"., 2000, pp. 701.", "H. Firouzabadi, S. Eslami, B. Karimi, \"Bull. Chem. Soc\". Jpn., vol. 74,\n2001, pp. 2401.\n[10] T. Kawabata, T. Mizugaki, K. Ebitani, K. Kaneda, \"Tetrahedron Lett\".\n2001, vol. 42, pp. 8329.\n[11] M. K. Basu, S. Samajdar, F. F. Becker, B. K. Banik, \"Syn. lett\" 2002, pp.\n319.\n[12] S. Palaniappan, P. Narender, C. Saravanan, V. J. Rao, \"Syn. Lett\"., 2003,\npp. 1793.\n[13] T. S.Jin; G. sun, Y. W. Li; \"Green chem\" vol. 4, 2002.\n[14] T. S.Jin; G. sun, Y. W. Li; \"J chem res, synop\".vol. 1, 2003.\n[15] T.S.T. Li, J; F. Han,JH. Yang, T.S.Li,Ultrson.Sono chem10\" 2003 .\n[16] R.Nagarajan; G.J. Magesh,P.T. Perunal, Synthesis\", 2004, 69.\n[17] P.R. Singh; D.U. Singh;S .D. Samant, \"Synlett\" 2004, 1909.\n[18] B.Wang; L.M. Yang;J .S. Suo, \" Synlett\" 45. 2004.\n[19] B.Wang; Y. Gu, W.Gong. Y.Kang. L .Yng 45, 2004.\n[20] B.Wang; Y. G .L.yang J. Suo, J .yang, \"catal. lett\", vol 96, 2004.\n[21] B.Wang; Y.L. Gu; C .Luo, \"Synlett\" 45 2004.\n[22] B.Wang; L.M. Yang ;J .S. Suo, \" tetrahedron lett \", vol 44, 2004.\n[23] Sheldon, R. A.; Downing, R. S.; Appl. Catal. A: General\" 1999, pp. 189,\n163.\n[24] P, Salehi; M. M.Khodaei; M. A, Zolfigol; S, Sirouszadeh; \"Bull. Chem.\nSoc. Jpn\". 2003, vol 76, pp.1863.\n[25] T, Kawabata; T, Mizugaki; K, Ebitani.; K, Kaneda.; \"Tetrahedron Lett\".\n2001, vol 42, pp. 8329.\n[26] J. H, Clark; C. N, Rhodes. Clean synthesis using porous inorganic solid\ncatalysts and supported reagents. RSC Clean Technology Monographs,\nClark, J. H., Ed.; Cambridge\", 2000.\n[27] J. H, Clark Green Chemistry: challenges and opportunities. Green Chem.\n1999, vol 1, pp. 1-8.\n[28] P. T, Anastas; J. C , Warner . \"Green Chemistry\": Theory and Practice;\nOxford University Press: Oxford, 1998.\n[29] P, Tundo., P. T, Anastas ., Eds. \" Green Chemistry\": Challenging\nPerspectives; Oxford Science: Oxford, 1999.\n[30] D. C, Sherrington. Polymer-supported synthesis. \"In Chemistry of Waste\nMinimisation\"; Clark, J. H., Ed.; Blackie Academic: London, 1995; pp.\n141-200.\n[31] D. J, Macquarrie. Organically modified hexagonal mesoporous silicas -\nClean synthesis of catalysts and the effect of high loading and\nnoncatalytic second groups on catalytic activity of amine- derivatised\nmaterials. Green Chem. 1999. vol 1, pp.195-198.\n[32] J. H, Clark; D. J, Macquarrie.; Price. Modified silicas for clean\ntechnology \"J. Chem\" Soc. Dalton Trans. 2000, pp. 101-110.\n[33] J. S, Beck.; Kresge, C. T.; Leonowicz, M. E.; Roth, W. J.; Vartuli, J. C.\nOrdered \"mesoporous molecular sieves synthesized by a liquid-crystal\ntemplate mechanism\". Nature 1992, pp. 359, 710-712."]}

Al2(HPO4)3 was easily prepared and used as a solid acid in acetalization of carbonyl compounds at room temperature and under solvent-free conditions. The protection was done in short reaction times and in good to high isolated yields. The cheapness and availability of this reagent with easy procedure and work-up make this method attractive for the organic synthesis.

Keywords

Acetalization, carbonylcompounds, green condition, protection., acid catalysis

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