Impact of Solvent and Their Contaminants on Pd/C Catalyzed Suzuki-Miyaura Cross-Coupling Reactions

被引:1
|
作者
de Lambert de Boisjan, Alexandre [1 ]
Allemann, Christophe [1 ]
Fadini, Luca [2 ]
机构
[1] Univ Appl Sci Western Switzerland, HES SO, Bd Peroles 80, CH-1700 Fribourg, Switzerland
[2] Helsinn Adv Synth, Via Ind 24, CH-6710 Biasca, Switzerland
关键词
cross-coupling; palladium on charcoal; poisoning; solvent effects; solvent contaminants; Suzuki-Miyaura; CYCLOPENTYL METHYL-ETHER; BOND FORMATION; PALLADIUM; MECHANISMS; CHARCOAL; HECK;
D O I
10.1002/hlca.202100035
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The aim of this work was to understand if solvent contaminants can interfere in Suzuki's cross-coupling reactions and if it can explain the lack of robustness in industrial processes. For this purpose, several parameters were tested on the industrial model reaction between 2-bromonaphthalene and phenylboronic acid catalyzed by Pd/C. Best results were obtained using THF as solvent. Traces of the precursors of the used solvents, such as 2,3-dihydrofurane or maleic anhydride (100-300 ppm related to the solvent) strongly poisoned the reaction, decreasing the conversion significantly. This means that to ensure robust production, solvent quality must be analyzed at the ppm level. Fortunately, addition of triphenylphosphine can circumvent the catalyst poisoning.
引用
收藏
页数:11
相关论文
共 50 条
  • [21] Synthesis of biphenylamines via Suzuki-Miyaura cross-coupling reactions
    Maj, Anna M.
    Delaude, Lionel
    Demonceau, Albert
    Noels, Alfred F.
    [J]. TETRAHEDRON, 2007, 63 (12) : 2657 - 2663
  • [22] Scope of the Suzuki-Miyaura Cross-Coupling Reactions of Potassium Heteroaryltrifluoroborates
    Molander, Gary A.
    Canturk, Belgin
    Kennedy, Lauren E.
    [J]. JOURNAL OF ORGANIC CHEMISTRY, 2009, 74 (03): : 973 - 980
  • [23] Progress of Nickel-Catalyzed Suzuki-Miyaura Cross-Coupling Reactions of Phenol Derivatives
    Chen, Guojun
    Du, Jianshi
    [J]. CHINESE JOURNAL OF ORGANIC CHEMISTRY, 2014, 34 (01) : 65 - 80
  • [24] Suzuki-Miyaura reactions of arenediazonium salts catalyzed by Pd(0)/C. One-pot chemoselective double cross-coupling reactions
    Taylor, Rachel H.
    Felpin, Francois-Xavier
    [J]. ORGANIC LETTERS, 2007, 9 (15) : 2911 - 2914
  • [25] Pd/C-catalyzed one-pot Suzuki-Miyaura cross-coupling/hydrogenation of pyridine derivatives
    Pitna, Dinda B.
    Tanaka, Nao
    Usuki, Toyonobu
    [J]. JOURNAL OF HETEROCYCLIC CHEMISTRY, 2021, 58 (10) : 2039 - 2044
  • [26] Suzuki-Miyaura Cross-Coupling under Solvent-Free Conditions
    Asachenko, Andrey F.
    Sorochkina, Kristina R.
    Dzhevakov, Pavel B.
    Topchiy, Maxim A.
    Nechaev, Mikhail S.
    [J]. ADVANCED SYNTHESIS & CATALYSIS, 2013, 355 (18) : 3553 - 3557
  • [27] Pd-PEPPSI: Pd-NHC Precatalyst for Suzuki-Miyaura Cross-Coupling Reactions of Amides
    Lei, Peng
    Meng, Guangrong
    Ling, Yun
    An, Jie
    Szostak, Michal
    [J]. JOURNAL OF ORGANIC CHEMISTRY, 2017, 82 (13): : 6638 - 6646
  • [28] Nickel-catalyzed Suzuki-Miyaura cross-coupling of C-F bonds
    Zhang, Tianhao
    Nohira, Itsuki
    Chatani, Naoto
    [J]. ORGANIC CHEMISTRY FRONTIERS, 2021, 8 (14) : 3783 - 3787
  • [29] Cyrene as a Bio-Based Solvent for the Suzuki-Miyaura Cross-Coupling
    Wilson, Kirsty L.
    Murray, Jane
    Jamieson, Craig
    Watson, Allan J. B.
    [J]. SYNLETT, 2018, 29 (05) : 650 - 654
  • [30] Pd(OAc)2/DABCO-catalyzed Suzuki-Miyaura cross-coupling reaction in DMF
    Li, Jin-Heng
    Zhu, Qi-Ming
    Xie, Ye-Xiang
    [J]. TETRAHEDRON, 2006, 62 (47) : 10888 - 10895