Chinese Journal of Organic Chemistry ›› 2019, Vol. 39 ›› Issue (11): 3258-3263.DOI: 10.6023/cjoc201902031 Previous Articles Next Articles
收稿日期:
2019-02-26
发布日期:
2019-07-03
通讯作者:
李江
E-mail:lijiang@cup.edu.cn
基金资助:
Li Jianga*(), Wan Tonga, Zhang Junjiea, Fu Yaob
Received:
2019-02-26
Published:
2019-07-03
Contact:
Li Jiang
E-mail:lijiang@cup.edu.cn
Supported by:
Share
Li Jiang, Wan Tong, Zhang Junjie, Fu Yao. Iron-Catalyzed Selective Hydrogenation of Stearic Acid to Stearyl Alcohol[J]. Chinese Journal of Organic Chemistry, 2019, 39(11): 3258-3263.
![]() | |||||||
Entry | Catalyst | Conv./% | Yield b/% | Carbon balance | |||
C18-OH | C17 | C18 | C17-CHO | ||||
1 | — | 33.3 | 0.5 | 0.5 | 0.1 | 0.2 | 3.9 |
2 | 20% Fe-N-C@Al2O3-900 | >99 | 88.6 | 1.1 | 2.4 | 0.4 | 92.5 |
3 | 20% Fe-Al2O3-900 | 21.6 | 0.9 | 0.9 | 0.1 | 2.2 | 19.0 |
4 | N-C@Al2O3-900 | 42.3 | 0.5 | 0.5 | 0.4 | 0.4 | 4.3 |
5 | Al2O3 | 43.3 | 7.9 | 1.0 | 0.9 | 4.1 | 32.1 |
6 | 20% Fe-N-C@Al2O3-550 | 98.3 | 80.4 | 1.5 | 14.3 | 0 | 97.9 |
7 | 20% Fe-N-C@Al2O3-700 | 95.7 | 34.1 | 0.7 | 3.8 | 3.0 | 43.5 |
8 | 20% Fe-N-C@Al2O3-1100 | 97.1 | 47.9 | 1.6 | 11.8 | 2.6 | 65.8 |
9 | 20% Fe-N-C@SiO2-900 | 88.5 | 1.0 | 1.3 | 0.1 | 1.1 | 4.0 |
10 | 20% Fe-N-C-900 | 92.1 | 4.3 | 1.6 | 0.7 | 1.8 | 9.1 |
11 | 20% Fe-N-C@TiO2-900 | 66.9 | 3.6 | 0.9 | 0.4 | 3.0 | 11.8 |
12 | 20% Fe(NO3)3-N-C@Al2O3-900 | 80.6 | 10.8 | 1.2 | 0.6 | 2.2 | 18.4 |
13 | 20% Fe-phen-C@Al2O3-900 | 96.2 | 58.8 | 0.9 | 4.4 | 3.5 | 70.3 |
14 | 3% Fe-N-C@Al2O3-900 | 89.4 | 52.6 | 1.0 | 1.1 | 2.9 | 64.4 |
15 | 5% Fe-N-C@Al2O3-900 | 94.7 | 21.6 | 0.6 | 0.8 | 3.9 | 28.4 |
16 | 10% Fe-N-C@Al2O3-900 | 98.0 | 62.0 | 0.6 | 0.6 | 1.8 | 66.3 |
17 | 30% Fe-N-C@Al2O3-900 | 99.3 | 46.0 | 0.8 | 1.5 | 2.2 | 50.9 |
![]() | |||||||
Entry | Catalyst | Conv./% | Yield b/% | Carbon balance | |||
C18-OH | C17 | C18 | C17-CHO | ||||
1 | — | 33.3 | 0.5 | 0.5 | 0.1 | 0.2 | 3.9 |
2 | 20% Fe-N-C@Al2O3-900 | >99 | 88.6 | 1.1 | 2.4 | 0.4 | 92.5 |
3 | 20% Fe-Al2O3-900 | 21.6 | 0.9 | 0.9 | 0.1 | 2.2 | 19.0 |
4 | N-C@Al2O3-900 | 42.3 | 0.5 | 0.5 | 0.4 | 0.4 | 4.3 |
5 | Al2O3 | 43.3 | 7.9 | 1.0 | 0.9 | 4.1 | 32.1 |
6 | 20% Fe-N-C@Al2O3-550 | 98.3 | 80.4 | 1.5 | 14.3 | 0 | 97.9 |
7 | 20% Fe-N-C@Al2O3-700 | 95.7 | 34.1 | 0.7 | 3.8 | 3.0 | 43.5 |
8 | 20% Fe-N-C@Al2O3-1100 | 97.1 | 47.9 | 1.6 | 11.8 | 2.6 | 65.8 |
9 | 20% Fe-N-C@SiO2-900 | 88.5 | 1.0 | 1.3 | 0.1 | 1.1 | 4.0 |
10 | 20% Fe-N-C-900 | 92.1 | 4.3 | 1.6 | 0.7 | 1.8 | 9.1 |
11 | 20% Fe-N-C@TiO2-900 | 66.9 | 3.6 | 0.9 | 0.4 | 3.0 | 11.8 |
12 | 20% Fe(NO3)3-N-C@Al2O3-900 | 80.6 | 10.8 | 1.2 | 0.6 | 2.2 | 18.4 |
13 | 20% Fe-phen-C@Al2O3-900 | 96.2 | 58.8 | 0.9 | 4.4 | 3.5 | 70.3 |
14 | 3% Fe-N-C@Al2O3-900 | 89.4 | 52.6 | 1.0 | 1.1 | 2.9 | 64.4 |
15 | 5% Fe-N-C@Al2O3-900 | 94.7 | 21.6 | 0.6 | 0.8 | 3.9 | 28.4 |
16 | 10% Fe-N-C@Al2O3-900 | 98.0 | 62.0 | 0.6 | 0.6 | 1.8 | 66.3 |
17 | 30% Fe-N-C@Al2O3-900 | 99.3 | 46.0 | 0.8 | 1.5 | 2.2 | 50.9 |
[1] |
Huber G. W. Iborra S. Corma A. Chem. Rev. 2006 106 4044.
doi: 10.1021/cr068360d |
[2] |
Corma A. Iborra S. Velty A. Chem. Rev. 2007 107 2411.
doi: 10.1021/cr050989d |
[3] |
Yang Z. Fu Y. Guo Q. Chin. J. Org. Chem. 2015 35 273.
doi: 10.6023/cjoc201409012 |
杨 珍 傅 尧 郭 庆祥 有机化学 2015 35 273.
doi: 10.6023/cjoc201409012 |
|
[4] |
Jamil F. Al-Haj L. Al-Muhtaseb A. H. Al-Hinai M. A. Baawain M. Rashid U. Ahmad M. N. M. Rev. Chem. Eng. 2018 34 267.
doi: 10.1515/revce-2016-0026 |
[5] | Besson, M.; Gallezot, P.; Pinel, C. Chem. Rev. 2014, 114, 1827. |
[6] | Gupta S. Frost and Sullivan Market Insight 2004 11075449. |
[7] |
Adkins H. Folkers K. J. Am. Chem. Soc. 1931 53 1095.
doi: 10.1021/ja01354a042 |
[8] |
Toba M. Tanaka S.-I. Niwa S.-I. Mizukami F. Koppány Z. Guczi L. Cheah K.-Y. Tang T.-S. Appl. Catal., A 1999 189 243.
doi: 10.1016/S0926-860X(99)00281-1 |
[9] |
Mendes M. Santos O. Jordao E. Silva A. Appl. Catal., A 2001 217 253.
doi: 10.1016/S0926-860X(01)00613-5 |
[10] |
Takeda Y. Nakagawa Y. Tomishige K. Catal. Sci. Technol. 2012 2 2221.
doi: 10.1039/c2cy20302b |
[11] |
Takeda Y. Tamura M. Nakagawa Y. Okumura K. Tomishige K. ACS Catal. 2015 5 7034.
doi: 10.1021/acscatal.5b01054 |
[12] |
Ullrich J. Breit B. ACS Catal. 2018 8 785.
doi: 10.1021/acscatal.7b03484 |
[13] |
Manyar H. G. Paun C. Pilus R. Rooney D. W. Thompson J. M. Hardacre C. Chem. Commun. 2010 46 6279.
doi: 10.1039/c0cc01365j |
[14] |
Rozmysłowicz B. Kirilin A. Aho A. Manyar H. Hardacre C. Wärn J. Salmi T. Murzin D. Y. J. Catalysis 2015 328 197.
doi: 10.1016/j.jcat.2015.01.003 |
[15] |
Toyao T. Siddiki S. M. Touchy A. S. Onodera W. Kon K. Morita Y. Kamachi T. Yoshizawa K. Shimizu K. I. Chem.-Eur. J. 2017 23 1001.
doi: 10.1002/chem.201604762 |
[16] |
Kandel K. Chaudhary U. Nelson N. C. Slowing I. I. ACS Catal. 2015 5 6719.
doi: 10.1021/acscatal.5b01664 |
[17] |
Wu L. Li L. Li B. Zhao C. Chem. Commun. 2017 53 6152.
doi: 10.1039/C7CC01126A |
[18] |
Onyestyák G. Harnos S. Kalló D. Catal. Commun. 2011 16 184.
doi: 10.1016/j.catcom.2011.09.032 |
[19] |
Gao X. Tong D. Zhong H. Jin B. Jin F. Zhang H. RSC Adv. 2016 6 27623.
doi: 10.1039/C6RA01150K |
[20] |
Kong X. Fang Z. Bao X. Wang Z. Mao S. Wang Y. J. Catalysis 2018 367 139.
doi: 10.1016/j.jcat.2018.08.022 |
[21] |
Jia W. Xu G. Liu X. Zhou F. Ma H. Zhang Y. Fu Y. Energy Fuels 2018 32 8438.
doi: 10.1021/acs.energyfuels.8b01114 |
[22] |
Song S. Wang D. Di L. Wang C. Dai W. Wu G. Guan N. Li L. Chin. J. Catal. 2018 39 250.
doi: 10.1016/S1872-2067(17)63003-1 |
[23] |
Li J. Zhang J. Wang S. Xu G. Wang H. Vlachos D. G. ACS Catal. 2019 9 1564.
doi: 10.1021/acscatal.8b04967 |
[24] |
Jagadeesh R. V. Surkus A. Junge H. Pohl M. Radnik J. Rabeah J. Huan H. Schunemann V. Bruckner A. Beller M. Science 2013 342 1073.
doi: 10.1126/science.1242005 |
[25] |
Cui X. Li Y. Bachmann S. Scalone M. Surkus A. Junge K. Topf C. Beller M. J. Am. Chem. Soc. 2015 137 10652.
doi: 10.1021/jacs.5b05674 |
[26] |
Natte K. Neumann H. Jagadeesh R. V. Beller M. Nat. Commun. 2017 8 1344.
doi: 10.1038/s41467-017-01428-0 |
[27] |
Li J. Liu J. Zhou H. Fu Y. ChemSusChem 2016 9 1339.
doi: 10.1002/cssc.201600089 |
[28] |
Li J. Liu J. Liu H. Xu G. Zhang J. Liu J. Zhou G. Li Q. Xu Z. Fu Y. ChemSusChem 2017 10 1436.
doi: 10.1002/cssc.201700105 |
[29] |
Li J. Zhang J. Liu H. Liu J. Xu G. Liu J. Sun H. Fu Y. ChemistrySelect 2017 2 11062.
doi: 10.1002/slct.201701966 |
[30] |
Li J. Sun H. Liu J. X. Zhang J. J. Li Z. X. Fu Y. Mol. Catal. 2018 452 36.
doi: 10.1016/j.mcat.2018.03.014 |
[31] |
Leveneur J. Waterhouse G. I. N. Kennedy J. Metson J. B. Mitchell D. R. G. J. Phys. Chem. C 2011 115 20978.
doi: 10.1021/jp206357c |
[1] | Fang Xiaolong, Duan Ning, Zhang Min, Li Bin. Advances for Ruthenium Catalysts with Metal-Ligand Cooperation for Hydrogenation of Oxalates into Ethylene Glycol [J]. Chinese Journal of Organic Chemistry, 2020, 40(9): 2692-2701. |
[2] | Liu Jiahao, Han Jingjie, Yi Xiaoyi, Liu Chao, He Piao. Research Progress of Homogeneous Catalyst for the Dehydrogenation of Formic Acid [J]. Chinese Journal of Organic Chemistry, 2020, 40(9): 2658-2668. |
[3] | Zhang Lu, Liu Aiqin, Liu Huazheng, Wan Renzhong, Sun Shutao, Liu Lei. Catalytic Asymmetric Synthesis of β,γ-Alkynyl α-Amino Esters via Chemo- and Enantio-selective Transfer Hydrogenation [J]. Chinese Journal of Organic Chemistry, 2020, 40(9): 2904-2911. |
[4] | Li Shengnan, Zhao Wenxin, Liu Yujing, Liu Zhongqiu, Ying Anguo. Research Progress in the Application of Supported Functional Ionic Liquids in Organic Transformations [J]. Chinese Journal of Organic Chemistry, 2020, 40(7): 1835-1846. |
[5] | Abdukader Ablimit, Wang Rong, Mamat Marhaba, Liu Chenjiang. FeCl2-Catalyzed Intramolecular Aerobic Reaction for Construction of Isoxazoles Heterocycle [J]. Chinese Journal of Organic Chemistry, 2020, 40(6): 1697-1703. |
[6] | Liu Yuanhua, Dong Xiu-Qin, Zhang Xumu. Recent Advances of Nickel-Catalyzed Homogeneous Asymmetric Hydrogenation [J]. Chinese Journal of Organic Chemistry, 2020, 40(5): 1096-1104. |
[7] | Sun Yue, Guan Rui, Liu Zhaohong, Wang Yeming. Recent Advances in Hydroboration of Alkenes Catalyzed by Fe, Co and Ni [J]. Chinese Journal of Organic Chemistry, 2020, 40(4): 899-912. |
[8] | Gu Guoxian, Hu Yang, Liu Shaodong, Dong Xiu-Qin, Zhang Xumu. Indan-f-amphox: An Efficient PNN Ligand for Iridium-Catalyzed Asymmetric Hydrogenation of β-Aryl β-Ketoesters [J]. Chinese Journal of Organic Chemistry, 2020, 40(4): 997-1002. |
[9] | Zhang Qiying, Zhang Yiming, Hao Erjun, Bai Juan, Qu Guirong, Guo Haiming. Asymmetric Transfer Hydrogenation via Dynamic Kinetic Resolution for the Construction of Carbocyclic N3-Purine Nucleosides [J]. Chinese Journal of Organic Chemistry, 2020, 40(2): 376-383. |
[10] | Yang Xiaohui, Gu Xuesong, Bin Huaiyu, Xie Jianhua, Zhou Qilin. Asymmetric Synthesis of (-)-Indolizidine167B and (+)-Coniine [J]. Chinese Journal of Organic Chemistry, 2020, 40(11): 3963-3968. |
[11] | Liu Jian, Xiao Jie, Mondal Sudipta, Leng Xuebing, Deng Liang. Reactions of Iron(II) Complexes Supported by Tripodal Amido-Phosphine-Amido Ligands with Diazo Compounds [J]. Chinese Journal of Organic Chemistry, 2020, 40(10): 3380-3389. |
[12] | Fang Xiaolong, Zhang Min, Duan Ning, Wang Xin, Zhu Hongping. Synthesis and Catalytic Property of New Aminophosphino Ruthenium Carbonyl Complexes [J]. Chinese Journal of Organic Chemistry, 2020, 40(1): 226-231. |
[13] | Yan Shiqiang, Dong Daoqing, Xie Chunwen, Wang Wensheng, Wang Zuli. Synthesis of Bicyclic ortho-Aminocarbonitrile Derivatives Catalyzed by 1,4-Diazabicyclo[2.2.2]octane [J]. Chin. J. Org. Chem., 2019, 39(9): 2560-2566. |
[14] | Zhang Xiang, Guo Caihong, Wu Haishun. Recent Developments of Homogeneous Transition-Metal Catalysts for Low Temperature Dehydrogenation of Methanol [J]. Chin. J. Org. Chem., 2019, 39(9): 2458-2466. |
[15] | Zhou Qiwen, Feng Xiangqing, Yang Jing, Du Haifeng. Asymmetric Transfer Hydrogenations of β-Enamine Cyanide with Chiral Ammonia Borane [J]. Chin. J. Org. Chem., 2019, 39(8): 2188-2195. |
Viewed | ||||||
Full text |
|
|||||
Abstract |
|
|||||