SciELO - Scientific Electronic Library Online

 
vol.55 issue3Application of Infrared Spectroscopy to the Monitoring of Lactose and Protein From Whey After Ultra and Nano Filtration Process author indexsubject indexsearch form
Home Pagealphabetic serial listing  

Services on Demand

Journal

Article

Indicators

Related links

  • Have no similar articlesSimilars in SciELO

Share


Journal of the Mexican Chemical Society

Print version ISSN 1870-249X

J. Mex. Chem. Soc vol.55 n.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.

 

DESCARGAR ARTÍCULO EN FORMATO PDF

 

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 ]

Creative Commons License All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License