Articles

Effective Transformation of Alkynylphosphonates into β-Ketophosphonates with a Silver(I) Catalyst

  • Liu Kaijian ,
  • Ou Jinhua ,
  • Ou Lijuan ,
  • Liu Hongwei ,
  • Tang Xinde ,
  • Li Laibing ,
  • Hu Bonian
Expand
  • Department of Materials and Chemical Engineering, Hunan Institute of Technology, Hengyang 421002

Received date: 2015-02-08

  Revised date: 2015-05-01

  Online published: 2015-07-10

Supported by

Project supported by the Science and Technology Planning Project of Hunan Province (No. 2014FJ3053), the National Natural Science Foundation of China (No. 21176061), the Natural Science Foundation of Hunan Province (No. 13JJ3132), the Construct Program of the Key Discipline in Hunan Province and Science and Technology Planning Project of Hengyang City (No. 2014KJ26).

Abstract

β-Ketophosphonates are an important class of carbonyl compounds which exhibit a wide range of biological activities and outstanding metal-complexing abilities. They are building blocks in organic synthesis, especially as intermediates for the synthesis of α,β-unsaturated carbonyl compounds, chiral β-hydroxy and β-hydroxy phosphonic acids. In this paper, a cheap, simple, convenient and environmentally benign method to synthesize the β-ketophosphonates from alkynylphosphonates was developed, which can be easily prepared in one step from commercial terminal alkynes. In the presence of 10 mol% AgOAc and 4 equiv. of water in methanol at 110 ℃, a broad range of alkynylphosphonates were converted into the corresponding β-ketophosphonates in nearly equivalent conversion through silver/methanol-catalyzed hydration reaction. The presented methodology will provide new strategies for β-ketophosphonates-type natural product and drug synthesis, which has important academic significance and application value.

Cite this article

Liu Kaijian , Ou Jinhua , Ou Lijuan , Liu Hongwei , Tang Xinde , Li Laibing , Hu Bonian . Effective Transformation of Alkynylphosphonates into β-Ketophosphonates with a Silver(I) Catalyst[J]. Chinese Journal of Organic Chemistry, 2015 , 35(9) : 1889 -1896 . DOI: 10.6023/cjoc201502015

References

[1] Lentsch, L. M.; Wiemer, D. F. J. Org. Chem. 1999, 64, 5205.
[2] Liu, Y.-L.; Liang, Y.; Pi, S.-F.; Li, J.-H. J. Org. Chem. 2009, 74, 5691.
[3] Kondoh, A.; Yorimitsu, H.; Oshima, K. Chem. Asian J. 2010, 5, 398.
[4] Atmani, A.; Memmou, F.; Bouillon, J.-P. Cr. Chim. 2009, 12, 963.
[5] Whitten, J. P.; Cube, R. V.; Baron, B. M.; McDonald, I. A. Bioorg. Med. Chem. Lett. 1993, 3, 19.
[6] Liu, P.; Liu, A.; Yan, F.; Wolfe, M. D.; Lipscomb, J. D.; Liu, H.-W. Biochemistry 2003, 42, 11577.
[7] Li, X.; Bhandari, A.; Holmes, C. P.; Szardenings, A. K. Bioorg. Med. Chem. Lett. 2004, 14, 4301.
[8] Balg, C.; Blais, S. P.; Bernier, S.; Huot, J. L.; Couture, M.; Lapointe, J.; Chênevert, R. Biorg. Med. Chem. 2007, 15, 295.
[9] Perumal, S. K.; Adediran, S. A.; Pratt, R. F. Biorg. Med. Chem. 2008, 16, 6987.
[10] Maryanoff, B. E.; Reitz, A. B. Chem. Rev. 1989, 89, 863.
[11] Pronin, S. V.; Martinez, A.; Kuznedelov, K.; Severinov, K.; Shuman, H. A.; Kozmin, S. A. J. Am. Chem. Soc. 2011, 133, 72.
[12] Yang, W.; Yu, Y.; Zhang, T.; Hansmann, M. M.; Pflästerer, D.; Hashmi, A. S. K. Adv. Synth. Catal. 2013, 355, 2037.
[13] Kitamura, M.; Tokunaga, M.; Noyori, R. J. Am. Chem. Soc. 1995, 117, 2931.
[14] Chívez, M. Á.; Vargas, S.; Suírez, A.; Álvarez, E.; Pizzano, A. Adv. Synth. Catal. 2011, 353, 2775.
[15] Ryglowski, A.; Kafarski, P. Tetrahedron 1996, 52, 10685.
[16] McCabe, D. J.; Duesler, E. N.; Paine, R. T. Inorg. Chem. 1985, 24, 4626.
[17] Koprowski, M.; Szymańska, D.; Bodzioch, A.; Marciniak, B.; Ró?ycka-Soko?owska, E.; Ba?czewski, P. Tetrahedron 9, 65, 4017.
[18] Maloney, K. M.; Chung, J. Y. L. J. Org. Chem. 2009, 74, 7574.
[19] Demmer, C. S.; Krogsgaard-Larsen, N.; Bunch, L. Chem. Rev. 2011, 111, 7981.
[20] Wei, W.; Ji, J.-X. Angew. Chem., Int. Ed. 2011, 50, 9097.
[21] Beller, M.; Seayad, J.; Tillack, A.; Jiao, H. Angew. Chem., Int. Ed. 2004, 43, 3368.
[22] Hintermann, L.; Labonne, A. Synthesis 2007, 1121.
[23] Zeng, X. Chem. Rev. 2013, 113, 6864.
[24] Xie, L. Y.; Yuan R.; Wang R. J.; Peng, Z. H.; Xiang, J. N.; He, W. M. Eur. J. Org. Chem. 2014, 13, 2668.
[25] Sturtz, C. C. G.; Normant, H. Bull. Soc. Chim. Fr. 1966, 1707.
[26] Li, X.; Hu, G.; Luo, P.; Tang, G.; Gao, Y.; Xu, P.; Zhao, Y. Adv. Synth. Catal. 2012, 354, 2427.
[27] Liu, K. J.; Liu, H. W.; Wang, W. G.; Ou, L. J.; Wang, J. J.; Hu, B. N. Chin. J. Org. Chem. 2014, 34, 2007 (in Chinese).(刘开建, 刘宏伟, 王文革, 欧丽娟, 王津津, 胡波年, 有机化学, 2014, 34, 2007.)
[28] Liu, K. J. Chem. J. Chin. Univ. 2014, 35, 1236 (in Chinese).(刘开建, 高等学校化学学报, 2014, 35, 1236.)
[29] Leyva, A.; Corma, A. J. Org. Chem. 2009, 74, 2067.
[30] Thuong, M. B. T.; Mann, A.; Wagner, A. Chem. Commun. 2012, 48, 434.
[31] Luke, G. P.; Seekamp, C. K.; Wang, Z.-Q.; Chenard, B. L. J. Org. Chem. 2008, 73, 6397.
[32] Moorhoff, C. M. Synth. Commun. 2003, 33, 2069.
Orsini, F.; Teodoro, E. D.; Ferrari, M. Synthesis 2002, 1683.

Outlines

/