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Journal of the Mexican Chemical Society

versión impresa ISSN 1870-249X

J. Mex. Chem. Soc vol.55 no.3 Ciudad de México jul./sep. 2011

 

Article

 

Synthesis of Dialkyl 2–(4–oxopyridin–1(4H)–yl)dicarboxylates Through the Reaction of 4–hydroxypyridine and Dialkyl Acetylenedicarboxylate in the Presence of Triphenylphosphine

 

Bita Mohtat,1* Zohre Najafi Azar,1 Semiramis Nahavandian,1 Hoorieh Djahaniani,2 and Abbas Ahmadi1

 

1 Department of Chemistry, Karaj Branch, Islamic Azad University, Karaj, Iran. *b.mohtat@jooyan.org

2 Department of Chemistry, East Tehran Branch, Islamic Azad University, Qiamdasht, Tehran, Iran.

 

Received March 16, 2011.
Accepted June 2, 2011.

 

Abstract

4–Hydroxypyridine undergoes a smooth reaction with dialkyl acetylenedicarboxylates in the presence of triphenylphosphine (15 mol %) to produce the E/Z isomers of dialkyl 2–(4–oxopyridin–1(4H)–yl)but–2–enedioates in high yields.

Keywords: 4–Hydroxypyridine, dialkyl acetylenedicarboxylates, triphenylphosphine, dialkyl 2–(4–oxopyridin–1(4H)–yl)but–2–enedioates.

 

Resumen

4–Hidroxipiridina reacciona bajo condiciones suaves con acetilencarboxilatos de dialquilo en presencia de trietilfosfina (15% molar) para producer los isómeros E/Z de los 2–(4–oxopiridin–1(4H)–il)but–2–endioatos de dialquilo en rendimientos elevados.

Palabras clave: 4–Hidroxipiridina, acetilendicarboxilatos de dialquilo, trifenilfosfina, 2–(4–oxopiridin–1(4H)–il)but–2–endioatos de dialquilo.

 

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References

1. Winterfeldt, E. Angew. Chem. Int. Ed. Engl. 1967, 6, 423–434.         [ Links ]

2. Butterfield, P. J.; Tebby, J. C.; Griffiths, D. V. J. Chem. Soc, Perkin Trans. 1979, 1, 1189–1191.         [ Links ]

3. Acheson, R. M.; Plunkett, A. O. J. Chem. Soc. 1964, 2676–2683.         [ Links ]

4. Winterfeldt, E.; Dillinger, H. J. Chem. Ber. 1966, 99, 1558–1568.         [ Links ]

5. Winterfeldt, E.; Schumann, D.; Dillinger, H. J. Chem. Ber. 1969, 102, 1656–1664.         [ Links ]

6. Yavari, I.; Ramazani, A. Synth. Commun. 1997, 27, 1449–1454.         [ Links ]

7. Bayat, M.; Imanieh, H.; Hassanzadeh, F. Tetrahedron Lett. 2010, 51, 1873–1875.         [ Links ]

8. Yavari, I.; Souri, S.; Sirouspour, M.; Djahaniani, H.; Nasiri, F. Synthesis, 2005, 1761–1764.         [ Links ]

9. Yavari, I.; Bayat, M. Tetrahedron, 2003, 59, 2001–2005.         [ Links ]

10. Acheson, R. M.; Elmore, N. F. Adv. Heterocycl. Chem. 1978, 23, 263–285.         [ Links ]

11. Acheson, R. M.; Woolard, J. J. Chem. Soc. Perkin Trans. 1975, 1, 438–446.         [ Links ]

12. Yavari, I.; Alborzi, A. R.; Mohtat, B. J. Chem. Res. (S) 2007, 152–154.         [ Links ]

13. Mohtat, B.; Jabbar, S.; Ghasemi, A.; Yavari, I. J. Chem. Res. (S) 2008, 601–603.         [ Links ]

14. Mohtat, B.; Azimzadeh, S.; Djahaniani, H.; Pirhadi, L. S. Afr. J. Chem. 2010, 63, 204–206.         [ Links ]

15. Yavari, I.; Alborzi, A. R.; Mohtat, B.; Nourmoharnmadian, F. Synth. Commun. 2008, 38, 703–712.         [ Links ]

16. Eliel, E. L.; Wilen, S. H. Stereochemistry of organic compounds, John Wiley & Sons, Inc, New York, 1994, pp. 569 –70.         [ Links ]

17. Shen, Y. Ace. Chem. Res. 1998, 31, 584–592.         [ Links ]

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