Citation: Wang Jingjing, Li Feng, Xu Yan, Wang Juan, Wu Ziyan, Yang Chengyu, Liu Lantao. Catalytic Nucleophilic Addition of 3, 5-Dialkyl-4-nitroisoxazoles to Trifluoromethyl Ketones on Water[J]. Chinese Journal of Organic Chemistry, ;2018, 38(5): 1155-1164. doi: 10.6023/cjoc201709049 shu

Catalytic Nucleophilic Addition of 3, 5-Dialkyl-4-nitroisoxazoles to Trifluoromethyl Ketones on Water

Henan Engineering Laboratory of Green Synthesis for Pharmaceuticals, School of Chemistry and Chemical Engineering, Shangqiu Normal University, Shangqiu 476000

Corresponding author: Wang Jingjing, wangjingjing0918@163.com Liu Lantao, liult05@iccas.ac.cn
Received Date: 29 September 2017
Revised Date: 29 December 2017
Available Online: 10 May 2018
Fund Project: the National Natural Sciences Foundation of China 21572126the Key Science Research of Education Committee in Henan Province 15A150072the Key Scientific and Technological Project of Henan Province 172102210099the National Natural Sciences Foundation of China 21402116Project supported by the National Natural Sciences Foundation of China (Nos. 21402116, 21502111, 21572126), the Key Scientific and Technological Project of Henan Province (No. 172102210099) and the Key Science Research of Education Committee in Henan Province (No. 15A150072)the National Natural Sciences Foundation of China 21502111

Figures(3)

The triethylamine catalyzed nucleophilic addition of 3, 5-dialkyl-4-nitroisoxazoles to trifluoromethyl ketones on water has been realized affording trifluoromethyl tertiary alcohol derivatives in 66%~99% yields. The products were easily transformed to the resulting alkenes by dehydration or acids by oxidation.
- on water,
- nucleophilic addition,
- 3, 5-dialkyl-4-nitroisoxazoles,
- trifluoromethyl ketones References
1. [1]
  (a) Welch, J. T. ; Eswarakrishman, S. Fluorine in Bioorganic Chemistry, Wiley, New York, 1991.
  (b) Filler, R. ; Kobayashi, Y. ; Yagupolskii, L. M. Organofluorine Compounds in Medicinal Chemistry and Biomedical Applications, Elsevier, Amsterdam, 1993.
  (c) Banks, R. E. ; Smart, B. E. ; Tatlow, C. J. Organofluorine Chemistry: Principles and Comercial Applications, Springer, New York, 1994.
  (d) Hiyama, T. ; Kanie, K. ; Kusumoto, T. ; Morizawa, Y. ; Shimizu, M. Organofluorine Compounds: Chemistry and Applications, Springer-Verlag, Berlin, 2000.
  (e) Kirsch, P. Modern Fluoroorganic Chemistry, Wiley-VCH, Weinheim, 2005.
  (f) Uneyama, K. Organofluorine Chemistry, Blackwell, Oxford, 2007.
  (g) Ojima, I. Fluorine in Medicinal Chemistry and Chemical Biology, Wiley-Blackwell, Chichester, 2009.
2. [2]
  (a) Kirk, K. L. J. Fluorine Chem. 2006, 127, 1013.
  (b) Mîller, K. ; Faeh, C. ; Diederich, F. Science 2007, 317, 1881.
  (c) Purser, S. ; Moore, P. R. ; Swallow, S. ; Gouverneur, V. Chem. Soc. Rev. 2008, 37, 320.
  (d) Hagmann, W. K. J. Med. Chem. 2008, 51, 4359.
  (e) Berger, R. ; Resnati, G. ; Metrangolo, P. ; Weber, E. ; Hulliger, J. Chem. Soc. Rev. 2011, 40, 3496.
  (f) Ojima, I. J. Org. Chem. 2013, 78, 6358.
  (g) Fujiwara, T. ; O_Hagan, D. J. Fluorine Chem. 2014, 167, 16.
  (h) Wang, J. ; Sánchez-Roselló, M. ; Aceñ a, J. L. ; Pozo, C. ; Sorochinsky, A. E. ; Fustero, S. ; Soloshonok, V. A. ; Liu, H. Chem. Rev. 2014, 114, 2432.
  (i) Gillis, E. P. ; Eastman, K. J. ; Hill, M. D. ; Donnelly, D. J. ; Meanwell, N. A. J. Med. Chem. 2015, 58, 8315.
3. [3]
  (a) Pierce, M. E. ; Rodney, L. P. J. ; Radesca, L. A. ; Lo, Y. S. ; Silverman, S. ; Moore, J. R. ; Islam, Q. ; Choudhury, A. ; Fortunak, J. M. D. ; Nguyen, D. ; Luo, C. ; Morgan, S. J. ; Davis, W. P. ; Confalone, P. N. ; Chen, C. -Y. ; Tillyer, R. D. ; Frey, L. ; Tan, L. ; Xu, F. ; Zhao, D. ; Thompson, A. S. ; Corley, E. G. ; Grabowski, E. J. J. ; Reamer, R. ; Reider, P. J. J. Org. Chem. 1998, 63, 8536.
  (b) Corbett, J. W. ; Ko, S. S. ; Rodgers, J. D. ; Gearhart, L. A. ; Magnus, N. A. ; Bacheler, L. T. ; Diamond, S. ; Jeffrey, S. ; Klabe, R. M. ; Cordova, B. C. ; Garber, S. ; Logue, K. ; Trainor, G. L. ; Anderson, P. S. ; Erickson-Viitanen, S. K. J. Med. Chem. 2000, 43, 2019.
4. [4]
  Schenck, H. A.; Lenkowski, P. W.; Choudhury-Mukherjee, I.; Ko, S.-H.; Stables, J. P.; Patel, M. K.; Brown, M. L. Bioorg. Med. Chem. 2004, 12, 979. doi: 10.1016/j.bmc.2003.12.011
5. [5]
  Fandrick, D. R.; Reeves, J. T.; Bakonyi, J. M.; Nyalapatla, P. R.; Tan, Z.; Niemeier, O.; Akalay, D.; Fandrick, K. R.; Wohlleben, W.; Ollenberger, S.; Song, J. J.; Sun, X.; Qu, B.; Haddad, N.; Sanyal, S.; Shen, S.; Ma, S.; Byrne, D.; Chitroda, A.; Fuchs, V.; Narayanan, B. A.; Grinberg, N.; Lee, H.; Yee, N.; Brenner, M.; Senanayake, C. H. J. Org. Chem. 2013, 78, 3592. doi: 10.1021/jo400080y
6. [6]
  (a) Betageri, R. ; Zhang, Y. ; Zindell, R. M. ; Kuzmich, D. ; Kirrane, T. M. ; Bentzien, J. ; Cardozo, M. ; Capolino, A. J. ; Fadra, T. N. ; Nelson, R. M. ; Paw, Z. ; Shih, D. -T. ; Shih, C. -K. ; Zuvela-Jelaska, L. ; Nebozny, G. ; Thomson, D. Bioorg. Med. Chem. Lett. 2005, 15, 4761.
  (b) Barker, M. ; Clackers, M. ; Copley, R. ; Demaine, D. A. ; Humphreys, D. ; Inglis, G. G. A. ; Johnston, M. J. ; Jones, H. T. ; Haase, M. V. ; House, D. ; Loiseau, R. ; Nisbet, L. ; Pacquet, F. ; Skone, P. A. ; Shanahan, S. E. ; Tape, D. ; Vinader, V. M. ; Washington, M. ; Uings, I. ; Upton, R. ; McLay, I. M. ; Macdonald, S. J. F. J. Med. Chem. 2006, 49, 4216.
7. [7]
  (a) Sani, M. ; Viani, F. ; Binda, M. ; Zaffaroni, N. ; Zanda, M. Lett. Org. Chem. 2005, 2, 447.
  (b) Betageri, R. ; Gilmore, T. ; Kuzmich, D. ; Kirrane, T. M. ; Bentzien, J. ; Wiedenmayer, D. ; Bekkali, Y. ; Regan, J. ; Berry, A. ; Latli, B. ; Kukulka, A. J. ; Fedra, T. N. ; Nelson, R. N. ; Goldrick, S. ; Zuvela-Jelaska, L. ; Souza, D. ; Pelletier, J. ; Dinallo, R. ; Panzenbeck, M. ; Torcellini, C. ; Lee, H. ; Pack, E. ; Harcken, C. ; Nabozny, G. ; Thomson, D. S. Bioorg. Med. Chem. Lett. 2011, 21, 6842.
8. [8]
  Carceller, E.; Merlos, M.; Giral, M.; Balsa, D.; Garcıía-Rafanell, J.; Forn, J. J. Med. Chem. 1996, 39, 487. doi: 10.1021/jm950555i
9. [9]
  For reviews, see: (a) Nie, J. ; Guo, H. -C. ; Cahard, D. ; Ma, J. -A. Chem. Rev. 2011, 111, 455.
  (b) Kelly, C. B. ; Mercadante, M. A. ; Leadbeater, N. E. Chem. Commun. 2013, 49, 11133.
10. [10]
  For selected examples: (a) Hara, N. ; Tamura, R. ; Funahashi, Y. ; Nakamura, S. Org. Lett. 2011, 13, 1662.
  (b) Zhang, G. -W. ; Meng, W. ; Ma, H. ; Nie, J. ; Zhang, W. -Q. ; Ma, J. -A. Angew. Chem., Int. Ed. 2011, 50, 3538.
  (c) Cui, H. -F. ; Wang, L. ; Yang, L. -J. ; Nie, J. ; Zheng, Y. ; Ma, J. -A. Tetrahedron 2011, 67, 8470.
  (d) Li, X. -J. ; Xiong, H. -Y. ; Hua, M. -Q. ; Nie, J. ; Zheng, Y. ; Ma, J. -A. Tetrahedron Lett. 2012, 53, 2117.
  (e) Zheng, Y. ; Xiong, H. -Y. ; Nie, J. ; Hua, M. -Q. ; Ma, J. -A. Chem. Commun. 2012, 48, 4308.
  (f) Luo, R. ; Li, K. ; Hu, Y. ; Tang, W. Adv. Synth. Catal. 2013, 355, 1297.
  (g) Zong, H. ; Huang, H. ; Bian, G. ; Song, L. J. Org. Chem. 2014, 79, 11768.
  (h) Wang, L. ; Liu, N. ; Dai, B. ; Ma, X. ; Shi, L. RSC Adv. 2015, 5, 10089.
  (i) Jamal, Z. ; Teo, Y. -C. RSC Adv. 2015, 5, 26949.
  (j) Zhang, D. ; Tanaka, F. Adv. Synth. Catal. 2015, 357, 3458.
  (k) Tao, R. ; Yin, X. -J. ; Wang, K. -H. ; Niu, Y. -Z. ; Wang, Y. -L. ; Huang, D. -F. ; Su, Y. -P. ; Wang, J. -X. ; Hu, Y. -L. ; Fu, Y. ; Du, Z. -Y. Chin. Chem. Lett. 2015, 26, 1046.
  (l) Jing, Z. ; Bai, X. ; Chen, W. ; Zhang, G. ; Zhu, B. ; Jiang, Z. Org. Lett. 2016, 18, 260.
  (m) Lutete, L. M. ; Miyamoto, T. ; Ikemoto, T. Tetrahedron Lett. 2016, 57, 1220.
  (n) Cook, A. M. ; Wolf, C. Angew. Chem., Int. Ed. 2016, 55, 2929.
  (o) Lee, K. ; Silverio, D. L. ; Torker, S. ; Robbins, D. W. ; Haeffner, F. ; Mei, F. W. ; Hoveyda, A. H. Nat. Chem. 2016, 8, 768.
  (p) Matador, E. ; Monge, D. ; Fernández, R. ; Lassaletta, J. M. Green Chem. 2016, 18, 4042.
  (q) Mszar, N. W. ; Mikus, M. S. ; Torker, S. ; Haeffner, F. ; Hoveyda, A. H. Angew. Chem., Int. Ed. 2017, 56, 8736.
  (r) Noda, H. ; Amemiya, F. ; Weidner, K. ; Kumagai, N. ; Shibasaki, M. Chem. Sci. 2017, 8, 3260.
  (s) Bai, X. ; Zeng, G. ; Shao, T. ; Jiang, Z. Angew. Chem., Int. Ed. 2017, 56, 3684.
  (t) Zheng, Y. ; Tan, Y. ; Harms, K. ; Marsch, M. ; Riedel, R. ; Zhang, L. ; Meggers, E. J. Am. Chem. Soc. 2017, 139, 4322.
11. [11]
  Bandini, M.; Sinisi, R. Org. Lett. 2009, 11, 2093. doi: 10.1021/ol9005079
12. [12]
  Zhang, Y.; Wei, B.-W.; Zou, L.-N.; Kang, M.-L.; Luo, H.-Q.; Fan, X.-L. Tetrahedron 2016, 72, 2472. doi: 10.1016/j.tet.2016.03.072
13. [13]
  Czerwinski, P.; Molga, E.; Cavallo, L.; Poater, A.; Michalak, M. Chem. Eur. J. 2016, 22, 8089. doi: 10.1002/chem.201601581
14. [14]
  (a) Grieco, P. A. Organic Synthesis in Water, Blackie, London, 1998.
  (b) Lindstrom, U. M. Organic Reactions in Water: Principles, Strategies and Applications, Blackwell, Oxford, U. K., 2007.
  (c) Li, C. -J. ; Chan, T. -H. Comprehensive Organic Reactions in Aqueous Media, Wiley, New York, 2007.
15. [15]
  For selected reviews: (a) Lindstrom, U. M. Chem. Rev. 2002, 102, 2751.
  (b) Head-Gordon, T. ; Hura, G. Chem. Rev. 2002, 102, 2651.
  (c) Hayashi, Y. Angew. Chem., Int. Ed. 2006, 45, 8103.
  (d) Mase, N. ; Barbas Ⅲ, C. F. Org. Biomol. Chem. 2010, 8, 4043.
16. [16]
  For selected reviews: (a) Li, C. -J. Chem. Rev. 2005, 105, 3095.
  (b) Li, C. -J. ; Chen, L. Chem. Soc. Rev. 2006, 35, 68.
  (c) Chanda, A. ; Fokin, V. V. Chem. Rev. 2009, 109, 725.
  (d) Butler, R. N. ; Coyne, A. G. Chem. Rev. 2010, 110, 6302.
  (e) Simon, M. -O. ; Li, C. -J. Chem. Soc. Rev. 2012, 41, 1415.
  (f) Gawande, M. B. ; Bonifacio, V. D. B. ; Luque, R. ; Branco, P. S. ; Varma, R. S. Chem. Soc. Rev. 2013, 42, 5522.
  (g) Levin, E. ; Ivry, E. ; Diesendruck, C. E. ; Lemcoff, N. G. Chem. Rev. 2015, 115, 4607.
  (h) Butler, R. N. ; Coyne, A. G. Org. Biomol. Chem. 2016, 14, 9945.
17. [17]
  For selected examples: (a) Phippen, C. B. W. ; Beattie, J. K. ; McErlean, C. S. P. Chem. Commun. 2010, 46, 8234.
  (b) Fu, X. -P. ; Liu, L. ; Wang, D. ; Chen, Y. -J. ; Li, C. -J. Green. Chem. 2011, 13, 549.
  (c) Sakakura, A. ; Koshikari, Y. ; Akakura, M. ; Ishihara, K. Org. Lett. 2011, 14, 30.
  (d) Paladhi, S. ; Chauhan, A. ; Dhara, K. ; Tiwari, A. K. ; Dash, J. Green. Chem. 2012, 14, 2990.
  (e) Islam, S. ; Larrosa, I. Chem. Eur. J. 2013, 19, 15093.
  (f) Sengoden, M. ; Punniyamurthy, T. Angew. Chem. Int. Ed. 2013, 52, 572.
  (g) Paladhi, S. ; Bhati, M. ; Panda, D. ; Dash, J. J. Org. Chem. 2014, 79, 1473.
  (h) Thakur, P. B. ; Meshram, H. M. RSC Adv. 2014, 4, 5343.
  (i) Thakur, P. B. ; Meshram, H. M. RSC Adv. 2014, 4, 6019.
  (j) Yu, J. -S. ; Liu, Y. -L. ; Tang, J. ; Wang, X. ; Zhou, J. Angew. Chem. Int. Ed. 2014, 53, 9512.
  (k) Yang, F. ; Klumphu, P. ; Liang, Y. -M. ; Lipshutz, B. H. Chem. Commun. 2014, 50, 936.
  (l) Zhang, F. -Z. ; Tian, Y. ; Li, G. -X. ; Qu, J. J. Org. Chem. 2015, 80, 1107.
  (m) SaiPrathima, P. ; Srinivas, K. ; Mohan Rao, M. Green. Chem. 2015, 17, 2339.
  (n) Bhattacharjya, A. ; Klumphu, P. ; Lipshutz, B. H. Nat. Commun. 2015, 6, 7401.
  (o) Cho, B. S. ; Chung, Y. K. Chem. Commun. 2015, 51, 14543.
  (p) Xiao, J. ; Wen, H. ; Wang, L. ; Xu, L. ; Hao, Z. ; Shao, C. -L. ; Wang, C. -Y. Green Chem. 2016, 18, 1032.
  (q) Zhang, Y. ; Wei, B. -W. ; Lin, H. ; Zhang, L. ; Liu, J. -X. ; Luo, H. -Q. ; Fan, X. -L. Green Chem. 2015, 17, 3266.
  (r) Ren, N. ; Nie, J. ; Ma, J. -A. Green Chem. 2016, 18, 6609.
18. [18]
  (a) Wang, J. ; Kong, W. -G. ; Li, F. ; Liu, J. ; Shen, Q. ; Liu, L. ; Zhao, W. -X. Org. Biomol. Chem. 2015, 13, 5399.
  (b) Li, F. ; Wang, J. ; Xu, M. ; Zhao, X. ; Zhou, X. ; Zhao, W. -X. ; Liu, L. Org. Biomol. Chem. 2016, 14, 3981.
  (c) Wang, J. ; Li, F. ; Shen, Q. ; Pei, W. ; Zhao, W. -X. ; Liu, L. Synthesis 2016, 48, 441.
  (d) Wang, J. ; Li, F. ; Xie, H. ; Xu, M. ; Zhao, X. ; Liu, L. ; Zhao, W. -X. Appl. Organomet. Chem. 2017, 31, e3545.
19. [19]
  CCDC 1558716(3a) and CCDC 1559048(5) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Center via www.ccdc.cam.ac.uk/data_request/cif.
20. [20]
  (a) Creary, X. J. Org. Chem. 1987, 52, 5026.
  (b) Chong, J. M. ; Mar, E. K. J. Org. Chem. 1991, 56, 893.
  (c) Prakash, G. K. S. ; Panja, C. ; Vaghoo, H. ; Surampudi, V. ; Kultyshev, R. ; Mandal, M. ; Rasul, G. ; Mathew, T. ; Olah, G. A. J. Org. Chem. 2006, 71, 6806.
  (d) Cheng, H. ; Pei, Y. ; Leng, F. ; Li, J. ; Liang, A. ; Zou, D. ; Wu, Y. ; Wu, Y. Tetrahedron Lett. 2013, 54, 4483.
21. [21]
  (a) Adamo, M. F. A. ; Duffy, E. F. Org. Lett. 2006, 8, 5157.
  (b) Adamo, M. F. A. ; Suresh, S. Tetrahedron 2009, 65, 990.
  (c) Zhang, J. ; Liu, X. ; Ma, X. ; Wang, R. Chem. Commun. 2013, 49, 9329.
22. [22]
  Gao, J.-R.; Wu, H.; Xiang, B.; Yu, W.-B.; Han, L.; Jia, Y.-X. J. Am. Chem. Soc. 2013, 135, 2983. doi: 10.1021/ja400650m
23. [23]
  Fiandra, C. D.; Piras, L.; Fini, F.; Disetti, P.; Moccia, M.; Adamo, M. F. A. Chem. Commun. 2012, 48, 3863. doi: 10.1039/c2cc30401e
24. [24]
  McBee, E. T.; Kim, Y. S.; Braendlin, H. P. J. Am. Chem. Soc. 1962, 84, 3154. doi: 10.1021/ja00875a023
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