TY - JOUR
T1 - A novel magnetic nanoparticle as an efficient and recyclable heterogeneous catalyst for the Suzuki cross-coupling reaction
AU - Jin, Hui
AU - Cui, Mengyu
AU - Liu, Peiwen
AU - Wang, Zhuo
AU - Jin, Tongxia
AU - Yang, Yonghui
AU - Zhu, Weiping
AU - Qian, Xuhong
N1 - Publisher Copyright:
© 2024 The Royal Society of Chemistry.
PY - 2024/8/7
Y1 - 2024/8/7
N2 - Heterogeneous palladium catalysts are widely used in catalytic hydrogenation, oxidation, reduction, and coupling reactions due to their good stability, recyclability, and reusability. Based on the palladium ion fluorescent probe, a novel magnetically recyclable heterogeneous palladium catalyst Fe3O4@FSM@Pd was constructed and characterized, which is highly efficient and reusable for the Suzuki-Miyaura cross-coupling reaction. The subsequent series of Maitlis' filtration test, catalyst concentration-yield kinetic experiments, and phase trajectory experiments further demonstrated that Fe3O4@FSM@Pd catalyzed through a heterogeneous mechanism under selected reaction conditions. In addition, Fe3O4@FSM@Pd was applied to catalyze the synthesis of five intermediates of active pharmaceutical ingredients (APIs): valsartan, sonidegib, erdafitinib, tubulin inhibitor, and lumacaftor. Importantly, the palladium residue in the API intermediates synthesized with Fe3O4@FSM@Pd as catalyst was less than 1 ppm. Furthermore, Fe3O4@FSM@Pd is stable and can be reused at least 5 times without losing activity.
AB - Heterogeneous palladium catalysts are widely used in catalytic hydrogenation, oxidation, reduction, and coupling reactions due to their good stability, recyclability, and reusability. Based on the palladium ion fluorescent probe, a novel magnetically recyclable heterogeneous palladium catalyst Fe3O4@FSM@Pd was constructed and characterized, which is highly efficient and reusable for the Suzuki-Miyaura cross-coupling reaction. The subsequent series of Maitlis' filtration test, catalyst concentration-yield kinetic experiments, and phase trajectory experiments further demonstrated that Fe3O4@FSM@Pd catalyzed through a heterogeneous mechanism under selected reaction conditions. In addition, Fe3O4@FSM@Pd was applied to catalyze the synthesis of five intermediates of active pharmaceutical ingredients (APIs): valsartan, sonidegib, erdafitinib, tubulin inhibitor, and lumacaftor. Importantly, the palladium residue in the API intermediates synthesized with Fe3O4@FSM@Pd as catalyst was less than 1 ppm. Furthermore, Fe3O4@FSM@Pd is stable and can be reused at least 5 times without losing activity.
UR - https://www.scopus.com/pages/publications/85201762115
U2 - 10.1039/d4re00226a
DO - 10.1039/d4re00226a
M3 - 文章
AN - SCOPUS:85201762115
SN - 2058-9883
VL - 9
SP - 2954
EP - 2962
JO - Reaction Chemistry and Engineering
JF - Reaction Chemistry and Engineering
IS - 11
ER -