An efficient conversion of aldehydes to their corresponding acylals with P2O5/SiO2 under mild condition

Phosphorus, Sulfur and Silicon and the Related Elements

Volumn 179, Issue 1, 2004, Pages 19-24

  Mirjalili, Bibi Fatemeh ^a   Zolfigol, Mohammad Ali ^b   Bamoniri, Abdolhamid ^c  

^a YAZD UNIVERSITY   (Iran)

^b BU ALI SINA UNIVERSITY   (Iran)

^c UNIVERSITY OF KASHAN   (Iran)

Author keywords

1,1 diacetate; Acylals; Diphosphorous pentoxide

Indexed keywords

4 NITROBENZALDEHYDE; ACETAL DERIVATIVE; ALDEHYDE DERIVATIVE; BENZALDEHYDE DERIVATIVE; NITRO DERIVATIVE; SILICON DIOXIDE; UNCLASSIFIED DRUG;

ARTICLE; BIOTRANSFORMATION; CATALYSIS; CHEMICAL REACTION; DIELS ALDER REACTION; INFRARED SPECTROSCOPY; PROTON NUCLEAR MAGNETIC RESONANCE; ROOM TEMPERATURE; THIN LAYER CHROMATOGRAPHY;

EID: 0742287575     PISSN: 10426507     EISSN: None     Source Type: Journal    
DOI: 10.1080/10426500490256998     Document Type: Article

References (30)

1. M. A. Zolfigol, M. H. Zebarjadian, I. Mohammadpoor-Baltork, and M. Shamsipur, Synth. Commun., 32, 2803 (2002).
2. T. S. Jin, G. Sun, Y. W. Li, and T. S. Li, J. Chem. Res. (Synop), 30 (2003).
3. I. Mohammadpoor-Baltork and H. Aliyan, Synth. Commun., 29, 2741 (1999).
4. I. Mohammadpoor-Baltork and H. Aliyan, J. Chem. Res. (Synop), 272 (1999).
5. H. W. Pinnick, K. S. Kochhar, B. S. Bal, R. P. Deshpandy, and S. N. Rajadhyaksha, J. Org. Chem., 48, 1765 (1983).
6. a) B. B. Sinder and S. G. Amin, Synth. Commun., 8, 117 (1978);
7. b) G. Saucy, R. Marbet, H. Lindlar and O. Isler, Helv. Chim. Acta., 42, 1945 (1959).
8. I. Freeman and E. M. Karchefski, J. Chem. Eng. Data., 22, 355 (1977).
9. T. S. Jin, G. Sun, Y. W. Li, and T. S. Li, Green Chemistry, 4, 255 (2002).
10. B. Karimi, G. R. Ebrahimian, and H. Seradj, Synth. Commun. 32, 669 (2002).
11. I. Scribine, Bull. Soc. Chem. Fr., 1194 (1961).
12. a) K. S. Kochhar, B. S. Bal, R. P. Deshpande, S. N. Rajadhyaksha, and H. W. Pinnick, J. Org. Chem., 48, 1765 (1983);
13. b) C. Wang and M. Li, Synth. Commun., 32, 3469 (2002).
14. J. K. Michie and J. A. Miller, Synthesis, 824 (1981).
15. N. Deka, D. J. Kalita, R. Borah, and J. C. Sarma, J. Org. Chem., 62, 1563 (1997).
16. V. K. Aggarwal, S. Fonquerna, and G. P. Vennall, Synlett, 849 (1998).
17. K. L. Chandra, P. Saravanan, and V. K. Singh, Synlett, 3, 359 (2000).
18. M. D. Carrigan, K. J. Eash, M. C. Oswald, and R. S. Mohan, Tetrahedron Lett., 42, 8133 (2001).
19. J. S. Yadav, B. V. S. Reddy, C. Venugopal, and T. Ramalingam, Synlett, 4, 604 (2002).
20. B. Karimi, H. Seradj, and G. R. Ebrahimian, Synlett, 5, 623 (2000).
21. G. A. Olah and A. K. Mehrotra, Synthesis, 962 (1982).
22. B. Gigante, C. Pereira, M. J. Marcelo-Curto, H. Carreyre, G. Perot, and M. Guisnet, Synthesis, 1077 (1995).
23. T. S. Jin, G. Y. Du, Z. H. Zhang, and T. S. Li, Synth. Commun., 27, 2261 (1997).
24. Z. H. Zhang, T. S. Li, and C. G. Fu, J. Chem. Res. (Synop), 174 (1997).
25. B. P. Bandgar, N. P. Mahajan, D. P. Mulay, J. L. Thote, and P. P. Wadgaonkar, J. Chem. Res. (Synop), 470 (1995).
26. M. Curini, F. Epifano, M. C. Marcotullio, O. Rosati, and M. Nocchetti, Tetrahedron Lett., 43, 2709 (2002).
27. N. M. Nagy, M. A. Jakab, J. Konya, and S. Antus, Applied Clay Science, 21, 213 (2002).
28. J. March, Advanced Organic Chemistry (Wiely, New York, 1985), 3rd ed., p. 904.
29. C. L. Eaton, J. Org. Chem., 38, 4071 (1973).
30. H. Eshghi, M. Rafei, and M. H. Karimi, Synth. Commun., 31, 771 (2001).