氮掺杂碳材料负载Pd纳米结构催化剂催化硝基芳烃与苄醇借氢还原偶联制备亚胺
收稿日期: 2020-07-19
修回日期: 2020-08-17
网络出版日期: 2020-09-09
基金资助
山东省重点研发计划(2019GGX102075)
Borrowing Hydrogen Reductive Coupling of Nitroarenes with Benzyl Alcohols to Imines Catalyzed by Pd Nanoparticles on N Doped Carbon Materials
Received date: 2020-07-19
Revised date: 2020-08-17
Online published: 2020-09-09
Supported by
the Key Technology R & D Program of Shandong Province(2019GGX102075)
车佳宁 , 宋涛 , 高先池 , 杨勇 . 氮掺杂碳材料负载Pd纳米结构催化剂催化硝基芳烃与苄醇借氢还原偶联制备亚胺[J]. 有机化学, 2021 , 41(1) : 276 -283 . DOI: 10.6023/cjoc202007046
Imines as a versatile organic synthetic intermediates have important applications in pharmaceuticals, dyes, and fine chemicals. In this work, heterogeneous Pd nanoparticles (Pd@N,O-carbon) on N doped carbon materials were developed using bamboo shoot as raw materials for highly efficient reductive coupling of nitroarenes with alcohols to selectively synthesize imines via the borrowing hydrogen strategy. The catalyst has obvious advantages in catalytic performance compared with other commercial catalysts or supports. Meanwhile, a broad set of complex imines were successfully synthesized in good yields with various functional groups tolerance for both nitroarenes and alcohols. This heterogeneous catalyst can also be recycled at several times without significant loss in activity and selectivity.
[1] | Adams, J.P. J. Chem. Soc., Perkin Trans. 1 2000, 125. |
[1] | Hadjipavlou-Litina, D.J.; Geronikaki, A.A. Drug Des. Discovery 1998, 15, 199. |
[2] | Su, F.; Mathew, S.C.; Mohlmann, L.; Antonietti, M; Wang, X.; Blechert, S. Angew. Chem., Int. Ed. 2012, 51, 657. |
[2] | Largeron, M.; Feury, M.-B. Angew. Chem., Int. Ed. 2011, 50, 5409. |
[2] | Schümperli, M.T.; Hammond, C.; Hermans, I. ACS Catal. 2012, 2, 1108. |
[2] | Biswas, S.; Dutta, B.; Mullick, K.; Kuo, C.H.; Poyraz, A.S.; Suib, S.L. ACS Catal. 2015, 5, 4394. |
[2] | Yuan, H.; Yoo, W.-J.; Miyamura, H.; Kobayashi, S. J. Am. Chem. Soc. 2012, 134, 13970. |
[2] | Chen, B.; Wang, L.-Y.; Gao, S. ACS. Catal. 2015, 5, 5851. |
[2] | Geng, L.L.; Song, J.J.; Zheng, B.; Wu, S.J.; Zhang, W.X.; Jia, M.J.; Liu, G. Chin. J. Catal. 2016, 37, 1451. |
[2] | Tamura, M.; Tomishige, K. Angew. Chem., Int. Ed. 2015, 54, 864. |
[2] | Liu, D; Zhang, C.H.; Du, M.M.; Zhang, X.L.; Zhao, P.S.; Yang, P. Chin. J. Org. Chem. 2018, 38, 1350. |
[2] | (刘迪, 张成慧, 韩楠, 杜萌萌, 张效露, 赵朋杉, 杨萍, 有机化学, 2018, 38, 1350.). |
[3] | Corma, A.; Navas, J.; Sabater, M.J. Chem. Rev. 2018, 118, 1410. |
[3] | Obora, Y. ACS Catal. 2014, 4, 3972. |
[3] | Guillena, G.; Ramon, D.; Yus, M. Chem. Rev. 2010, 110, 1611. |
[4] | Das, K.; Shibuya, R.; Nakahara, Y.; Germain, N.; Ohshima, T.; Mashima, K. Angew. Chem., Int. Ed. 2012, 51, 150. |
[4] | Dang, T.T.; Ramalingam, B.; Shan, S.P.; Seayad, A.M. ACS Catal. 2013, 3, 2536. |
[4] | Maji, M.; Chakrabarti, K.; Paul, B.; Roy, B.C.; Kundu, S. Adv. Synth. Catal. 2018, 360, 722. |
[4] | Imm, S.; Bahn, S.; Neubert, L.; Neumann, H.; Beller M.Angew. Chem. Int. Ed. 2010, 49, 8126. |
[4] | Pingen, D.; Müller, C.; Vogt, D. Angew. Chem., Int. Ed. 2010, 49, 8130. |
[4] | Cano, R.; Ramon, D.J.; Yus, M. J. Org. Chem. 2011, 76, 5547. |
[4] | Hamid, M.H.S. A.; Allen, C.L.; Lamb, G.W.; Maxwell, A.C.; Maytum, H.C.; Watson, A.J.A.; Williams, J.M.J.J. Am. Chem. Soc. 2009, 131, 1766. |
[4] | Kawahara, R.; Fujita, K.-I.; Yama-guchi, R. J. Am. Chem. Soc. 2010, 132, 15108. |
[4] | Ruch, S.; Irrgang, T.; Kempe, R. Chem. -Eur. J. 2014, 20, 13279. |
[4] | Saidi, O.; Blacker, A.J.; Farah, M.M.; Marsden, S.P.; Williams, J.M.J. Chem. Commun. 2010, 46, 1541. |
[4] | Gunanathan, C.; Milstein, D. Angew. Chem., Int. Ed. 2008, 47, 8661. |
[4] | Yan, T.; Feringa, B.L.; Barta, K. Nat. Commun. 2014, 5, 5602. |
[4] | Rawlings, A.J.; Diorazio, L.J.; Wills, M. Org. Lett. 2015, 17, 1086. |
[4] | Mukherjee, A.; Nerush, A.; Leitus, G.; Shimon, L.J.W.; David, Y.B.; Jalapa, N.A.E.; Milstein, D. J. Am. Chem. Soc. 2016, 138, 4298. |
[4] | Elangovan, S.; Neumann, J.; Sortais, J.-B.; Junge, K.; Darce, C.; Beller M.Nat. Commun. 2016, 7, 12641. |
[4] | Rosler, S.; Ertl, M.; Irrgang, T.; Kempe, R. Angew. Chem., Int. Ed. 2015, 54, 15046. |
[4] | Mastalir, M.; Tomsu, G.; Pittenauer, E.; Allmaier, G.; Kirchner, K. Org. Lett. 2016, 18, 3462. |
[4] | Lu, X.L.; Zhang, L.; Gu, X.L.; Liu, Y.X. Fine Chem. 2013, 44, 29. |
[4] | (r) Yang, P.; Liu, M.; Zhang, H.; Guo, W.; Lv, C.; Liu, D. Prog. Chem. 2020, 32, 72. |
[5] | Tang, L.; Sun, H.; Li, Y.; Zha, Z.; Wang, Z. Green Chem. 2012, 14, 3423. |
[5] | Chen, J.; Huang, S.; Lin, J.; Su, W. Appl. Catal. A 2014, 470, 1. |
[6] | J. J. G. J.; Duan, Y. N.; Zhang, S. C.; Fei, B. H.; Chen, X. F.; Yang, Y.ChemSusChem 2017, 10, 3427. |
[6] | Duan, Y. N.; Ji, G. J.; Zhang, S. C.; Chen, X. F.; Yang, Y.Catal. Sci. Technol. 2018, 8, 1039. |
[7] | Ji, G.J. ; Duan, Y.N. ; Zhang, S.C. Yang, Y. Catal. Today 2019 , 15 , 101. |
[8] | Song, T. ; Duan, Y. ; Yang, Y. Catal. Commun . 2019 , 120 , 80. |
[9] | Yu, L.; Huang, Y.; Wei, Z.; Ding, Y.; Su, C.; Xu, Q. J. Org. Chem. 2015, 80, 8677. |
[9] | Zhang, D.; Wei, Z.; Yu, L. Sci. Bull. 2017, 62, 1325. |
[10] | Chen, Y.; Jing, X.; Yu, L. Chin. J. Org. Chem. , 2020, 40, 2570. |
[10] | (陈颖, 景崤壁, 俞磊, 有机化学, 2020, 40, 2570.). |
[10] | Chen, Y.; Zhang, Q.; Jing, X.; Han, J.; Yu, L. Mater. Lett. 2019, 242, 170. |
[10] | Zhang, D.; Deng, X.; Zhang, Q.; Yu, L. Mater. Lett. 2019, 234, 216. |
[11] | Song, T. ; Duan, Y. ; Chen, X. ; Yang, Y. Catalysts 2019 , 9 , 116. |
[12] | Mohamad, T. ; Moomen, B. ; Fawaz, E. ; Amer, E. ; Mazen, E. ; Valerie, R. Asian J. Chem . 2006 , 18 , 1771. |
[13] | Roe, A. ; Montgomery, J.A. J. Am. Chem. Soc . , 1953 , 75 , 910. |
[14] | Torregros, R. ; Pastor, I.M. ; Yus, M. Tetrahedron 2005 , 61 , 11148. |
[15] | Benington, F. ; Morin, R.D. ; Clark, Leland, C., Jr. J. Org. Chem . 1958 , 23 , 19. |
[16] | Maginnity, P.M. ; Eisenmann, J.L. J. Am. Chem. Soc . 1952 , 74 , 6119. |
[17] | Hartley, J.H. ; Phillips, M.D. ; James, T.D. New J. Chem . , 2002 , 26 , 1228. |
[18] | Bennett, J.S. ; Charles, K.L. ; Miner, M.R. ; Heuberger, C.F. ; Spina, E.J. ; Bartels, M.F. ; Foreman, T. Green Chem . 2009 , 11 , 166. |
[19] | Steevens, J.B. ; Pandit, U.K. Tetrahedron 1983 , 39 , 1395. |
/
〈 |
|
〉 |