无金属条件下以酰基膦酸酯为烷基自由基受体的分子间酰化反应
收稿日期: 2022-07-30
修回日期: 2022-08-26
网络出版日期: 2022-09-09
基金资助
国家自然科学基金(22171200)
Intermolecular Acylation with Acylphosphonates as Alkyl Radical Receptor under Metal-Free Conditions
Received date: 2022-07-30
Revised date: 2022-08-26
Online published: 2022-09-09
Supported by
National Natural Science Foundation of China(22171200)
方晶 , 闵庆强 , 秦海涛 , 刘峰 . 无金属条件下以酰基膦酸酯为烷基自由基受体的分子间酰化反应[J]. 有机化学, 2022 , 42(12) : 4332 -4339 . DOI: 10.6023/cjoc202207044
As one of the central functional groups in organic chemistry, carbonyl skeleton can be achieved by many ways, but the intermolecular radical reaction using acyl phosphonate as acyl donor is rarely reported. The acylation reaction between acyl phosphonate as a free radical acceptor and three free radical donors, alkyl aldehyde, Hans ester and alkane, was studied under thermochemical and photochemical conditions, respectively. When alkyl aldehydes and alkanes were used as radical precursors, the intermolecular acylation reaction could proceed smoothly under the conditions of microwave heating and the presence of oxidants. When Hantzsch esters were used as the radical precursors, the intermolecular acylation reaction could take place smoothly under UV irradiation at room temperature.
| [1] | (a) Beller, M. Catalytic Carbonylation Reactions, Springer, Berlin, Heidelberg, 2006. |
| [1] | (b) Kolla?r, L. Modern Carbonylation Methods, Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim, 2008. |
| [1] | (c) Beller, M.; Bolm, C. Transition Metals for Organic Synthesis: Building Blocks and Fine Chemicals, Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim, 2008. |
| [2] | Xu, Z. Z. Fine Chem Raw Mater. Intermed. 2012, 2, 11. (in Chinese) |
| [2] | ( 徐兆瑜, 精细化工原料及中间体, 2012, 2, 11.) |
| [3] | (a) Li, Y. H.; Hu, Y. Y.; Wu, X. F. Chem. Soc. Rev. 2018, 47, 172. |
| [3] | (b) You, C.; Li, S. L.; Li, X. X.; Lan, J. L.; Yang, Y. H.; Chung, L. W.; Lv, H.; Zhang, X. M. J. Am. Chem. Soc. 2018, 140, 4977. |
| [3] | (c) Zhao, S. L.; Mankad, N. P. Catal. Sci. Technol. 2019, 9, 3603. |
| [3] | (d) Peltier, J. L.; Tomás-Mendivil, E.; Tolentino, D. R.; Hansmann, M. M.; Jazzar, R.; Bertrand, G. J. Am. Chem. Soc. 2020, 142, 18336. |
| [3] | (e) Bhattacherjee, D.; Rahman, M.; Ghosh, S.; Bagdi, A. K.; Zyryanov, G. V.; Chupakhin, O. N.; Das, P.; Hajra, A. Adv. Synth. Catal. 2021, 363, 1597. |
| [3] | (f) Yin, Z. P.; Shi, W. D.; Wu, X. F. J. Org. Chem. 2022, 54, 13941. |
| [4] | (a) Sekine, M.; Satoh, M.; Yamagata, H.; Hata, T. J. Org. Chem. 1980, 45, 4162. |
| [4] | (b) Sekine, M.; Kume, A.; Nakajima, M.; Hata, T. Chem. Lett. 1981, 1087. |
| [4] | (c) Sekine, M.; Kume, A.; Hata, T. Tetrahedron Lett. 1981, 37, 3617. |
| [4] | (d) Maeda, H.; Takahashi, K.; Ohmori, H. Tetrahedron 1988, 54, 12233. |
| [4] | (e) Takenaka, N.; Abell, J. P.; Yamamoto, H. J. Am. Chem. Soc. 2007, 129, 742. |
| [4] | (f) Martín, V. L.; Río-Rodríguez, R. D.; Díaz-Tendero, S.; Fernández-Salas, J. A.; Alemán, J. Chem. Commun. 2018, 54, 13941. |
| [4] | (g) Chang, X. F.; Wang, Q. F.; Wang, Y. M.; Song, H. B.; Zhou, Z. H.; Tang, C. C. Eur. J. Org. Chem. 2013, 2013, 2164. |
| [5] | (a) Kim, S.; Jon, S. Y. Chem. Commun. 1996, 1335. |
| [5] | (b) Neshchadin, D.; Rosspeintner, A.; Griesser, M.; Lang, B.; Mosquera-Vazquez, S.; Vauthey, E.; Gorelik, V.; Liska, R.; Hametner, C.; Ganster, B.; Saf, R.; Moszner, N.; Gescheidt, G. J. Am. Chem. Soc. 2013, 135, 17314. |
| [6] | (a) Kiyooka, S.; Kaneko, Y.; Matsue, H.; Hamada, M.; Fujiyama, R. J. Org. Chem. 1990, 55, 5562. |
| [6] | (b) Curran, D. P.; Liu, H. J. Org. Chem. 1991, 56, 3463. |
| [6] | (c) Curran, D. P.; Palovich, M. Synlett 1992, 631. |
| [6] | (d) Curran, D. P.; Diederichsen, U.; Palovich, M. J. Am. Chem. Soc. 1997, 119, 4797. |
| [6] | (e) Diederichsen, U.; Curran, D. P. J. Organomet. Chem. 1997, 531, 9. |
| [6] | (f) Pandey, G.; Tiwari, S. K.; Singh, B.; Vankab, K.; Jain, S. Chem. Commun. 2017, 53, 12337. |
| [6] | (g) Pandey, G.; Tiwari, S. K.; Singh, P.; Mondal, P. K. Org. Lett. 2021, 23, 7730. |
| [7] | For other carbonyl equivalent radical acceptors, see: (a) Iserloh, U.; Curran, D. P. J. Org. Chem. 1998, 63, 4711. |
| [7] | (b) Kim, S.; Lee, I. Y.; Yoon, J.-Y.; Oh, D. H. J. Am. Chem. Soc. 1996, 118, 5138. |
| [7] | (c) Clive, D. L. J.; Beaulieu, P. L.; Set, L. J. Org. Chem. 1984, 49, 1313. |
| [7] | (d) Bentrude, W. G.; Darnall, K. R. J. Am. Chem. Soc. 1968, 90, 3588. |
| [7] | (e) Kim, S.; Lim, K. C.; Kim, S.; Ryu, I. Adv. Synth. Catal. 2007, 349, 527. |
| [7] | (f) Zhu, Y. C.; Wen, X. J.; Song, S.; Jiao, N. ACS Catal. 2016, 6, 6465. |
| [7] | (g) Zeng, X. B.; Wang, X.; Zhang, Y. N.; Zhu, L.; Zhao, Y. Org. Biomol. Chem. 2020, 18, 3734. |
| [7] | (h) Wang, X. M.; Yu, M.; Song, H. J.; Liu, Y. X.; Wang, Q. M. Org. Lett. 2021, 23, 8353 |
| [8] | (a) Kajiwara, A.; Konishi, Y.; Morishima, Y.; Schnabel, W.; Kuwata, K.; Kamachi, M. Macromolecules 1993, 26, 1656. |
| [8] | (b) Jockusch, S.; Koptyug, I. V.; McGarry, P. F.; Sluggett, G. W.; Turro, N. J.; Watkins, D. M. J. Am. Chem. Soc, 1997, 119, 11495. |
| [8] | (c) Rees, M. T. L.; Russell, G. T.; Zammit, M. D.; Davis, T. P. Macromolecules 1998, 31, 1763. |
| [9] | (a) Kim, S.; Cho, C. H.; Lim, C. J. J. Am. Chem. Soc. 2003, 125, 9574. |
| [9] | (b) Goh, K. K. K.; Kim, S.; Zard, S. Z. Org. Lett. 2013, 15, 4818. |
| [9] | (c) Zhang, B. X.; He, J. Y.; Li, Y.; Song, T.; Fang, Y. W.; Li, C. Z. J. Am. Chem. Soc. 2021, 143, 4955. |
| [10] | Bonet, á. G.; Gaspar, A. F.; Martin, R. J. Am. Chem. Soc. 2013, 135, 12576. |
| [11] | Johannes, C. L. W.; Martin, O. Angew. Chem., Int. Ed. 2019, 58, 15386. |
| [12] | Zhang, X. Y.; Wang, Z. X.; Fan, X. S.; Wang, J. J. J. Org. Chem. 2015, 80, 10660. |
| [13] | Wang, L.; Wang, T.; Cheng, G. J.; Li, X. B.; Wei, J. J.; Guo, B.; Zheng, C. J.; Chen, G. Y.; Ran, C. Z.; Zheng, C. ACS Catal. 2020, 10, 7543. |
| [14] | Wang, C. A.; Rahman, M. M.; Bisz, E.; Dziuk, B.; Szostak, R.; Szostak, M. ACS Catal. 2022, 12, 2426. |
| [15] | Li, X. J.; Zou, G. J. Organomet Chem. 2015, 794, 136. |
| [16] | Pang, Y. B.; Liu, G. T.; Huang, C. C.; Yuan, X.-A.; Li, W. P.; Xie, J. Angew. Chem., Int. Ed. 2020, 59, 12789. |
| [17] | Allwood, D. M.; Blakemore, D. C.; Ley, S. V. Org. Lett. 2014, 16, 3064. |
| [18] | Polidano, K.; Allen, B. D. W.; Williams, J. M. J.; Morrill, L. C. ACS Catal. 2018, 8, 6440. |
| [19] | Dingwall, P.; Greb, A.; Crespin, L. N. S.; Labes, R.; Musio, B.; Poh, J.-S.; Pasau, P.; Blakemorec, D. C.; Ley, S. V. Chem. Commun. 2018, 54, 11685. |
| [20] | Sasano, Y.; Murakami, K.; Nishiyama, T.; Kwon, E.; Iwabuchi, Y. Angew. Chem., Int. Ed. 2013, 52, 12624. |
| [21] | Gao, K. C.; Xu, M.; Cai, C.; Ding, Y. H.; Chen, J. H.; Liu, B. S.; Xia, Y. Z. Org. Lett. 2020, 22, 6055. |
/
| 〈 |
|
〉 |