Synthesis of formamides containing unsaturated groups by N-formylation of amines using CO2 with H2

被引:79
|
作者
Liu, Hangyu [1 ,2 ]
Mei, Qingqing [1 ,2 ]
Xu, Qingling [2 ]
Song, Jinliang [1 ]
Liu, Huizhen [1 ,2 ]
Han, Buxing [1 ,2 ]
机构
[1] Chinese Acad Sci, Inst Chem, Beijing Natl Lab Mol Sci, CAS Key Lab Colloid & Interface & Thermodynam, Beijing 100190, Peoples R China
[2] Univ Chinese Acad Sci, Sch Chem & Chem Engn, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
COVALENT ORGANIC FRAMEWORKS; CARBON-DIOXIDE; AMBIENT CONDITIONS; ROOM-TEMPERATURE; IONIC LIQUIDS; CATALYST; HYDROGENATION; REDUCTION; FORMATE; CONVERSION;
D O I
10.1039/c6gc02243j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Formamides have wide applications in the industry and have been synthesized using CO2 as a carbon source and H-2 as a reducing agent. However, previous systems required a noble catalyst and high temperature to achieve high efficiency, and the substrate scope was mostly limited to saturated amines. The selective N-formylation of amines containing unsaturated groups using CO2 and H-2 is challenging because the efficient catalysts for the N-formylation are usually very active for hydrogenation of the unsaturated groups. Herein, we achieved for the first time a selective and efficient N-formylation of amines containing unsaturated groups using CO2 and H-2 with a Cu(OAc)(2)-4-dimethylaminopyridine (DMAP) catalytic system. The substrates were converted to the desired formamides, while the unsaturated groups, such as the carbonyl group, the C=C bond, C N bond and the ester group remained. The main reason for the excellent selectivity of the Cu(OAc)(2)-DMAP catalytic system was that it was very active for the N-formylation reaction, but was not active for the hydrogenation of the unsaturated groups.
引用
收藏
页码:196 / 201
页数:6
相关论文
共 50 条
  • [21] Borohydride Ionic Liquids as Reductants of CO2 in the Selective N-formylation of Amines
    Pachalska, Paulina
    Skarzynska, Anna
    Matias, Ines A. S.
    Trzeciak, Anna M.
    CHEMSUSCHEM, 2024, 17 (07)
  • [22] Triethylamine Catalyzed Reductive CO2 to Form N-Formylation of Amines and Hydrazides
    Wei, Xiu-Zhi
    Lu, Qiqi
    Liu, Jianguo
    Ma, Longlong
    CHEMISTRYSELECT, 2022, 7 (27):
  • [23] Bifunctional Ru-loaded Porous Organic Polymers with Pyridine Functionality: Recyclable Catalysts for N-Formylation of Amines with CO2 and H2
    Zhang, Kai
    Zong, Lingbo
    Jia, Xiaofei
    ADVANCED SYNTHESIS & CATALYSIS, 2021, 363 (05) : 1335 - 1340
  • [24] N-formylation of amines with CO2 by using Zr-based metal-organic frameworks: Contribution of defect sites of MOFs to N-formylation
    Yoo, Dong Kyu
    Jhung, Sung Hwa
    APPLIED CATALYSIS A-GENERAL, 2023, 659
  • [25] Iron-Catalyzed Selective N-Methylation and N-Formylation of Amines with CO2
    Li, Wen-Duo
    Zhu, Dao-Yong
    Li, Gang
    Chen, Jie
    Xia, Ji-Bao
    ADVANCED SYNTHESIS & CATALYSIS, 2019, 361 (22) : 5098 - 5104
  • [26] N-formylation of amines using phenylsilane and CO2 over ZnO catalyst under mild condition
    Wang, Pengbo
    He, Qian
    Zhang, Hao
    Sun, Qingdi
    Cheng, Yujie
    Gan, Tao
    He, Xiaohui
    Ji, Hongbing
    CATALYSIS COMMUNICATIONS, 2021, 149
  • [27] N-Formylation of amines using a domestic microwave oven and bioactivities of some N-formamides
    Mai, Nguyen Thi Ngoc
    Van Dat, Nguyen
    Huan, Trinh Thi
    Hoan, Duong Quoc
    VIETNAM JOURNAL OF CHEMISTRY, 2021, 59 (03) : 389 - 394
  • [28] Phosphonium-Salt-Catalyzed N-Methylation and N-Formylation of Amines with CO2
    Ren, Changyue
    Spannenberg, Anke
    Werner, Thomas
    ACS SUSTAINABLE CHEMISTRY & ENGINEERING, 2024, 12 (29): : 10969 - 10977
  • [29] Catalyst free N-formylation of aromatic and aliphatic amines exploiting reductive formylation of CO2 using NaBH4
    Kumar, Arun
    Sharma, Pankaj
    Sharma, Nidhi
    Kumar, Yashwant
    Mahajan, Dinesh
    RSC ADVANCES, 2021, 11 (41) : 25777 - 25787
  • [30] A DFT study unveils the secret of how H2 is activated in the N-formylation of amines with CO2 and H2 catalyzed by Ru(II) pincer complexes in the absence of exogenous additives
    Lu, Yu
    Liu, Zheyuan
    Guo, Jiandong
    Qu, Shuanglin
    Zhao, Ruihua
    Wang, Zhi-Xiang
    CHEMICAL COMMUNICATIONS, 2017, 53 (89) : 12148 - 12151