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- W4376642780 abstract "Higher amines are important high-valuable chemicals with wide applications, and amination of alcohols is a green route to them, which however generally suffers from harsh reaction conditions and use of equivalent base. Herein, we report an ionic-liquid (IL) hydrogen-bonding promoted dihydrogen autotransfer strategy for amination of alcohols to higher amines over cobalt catalyst under base-free conditions. Co(BF4 )2 ⋅ 6 H2 O complexed with triphos and IL (e. g., tetrabutylphosphonium tetrafluoroborate, [P4444 ][BF4 ]) shows high performances for the reaction and is tolerant of a wide scope of amines and alcohols, affording higher amines in good to excellent yields. Mechanism investigation indicates that the [BF4 ]- anion activates the alcohol via hydrogen bonding, promoting transfer of both hydroxyl H and α-H atoms of alcohol to the cobalt catalyst to form an aldehyde intermediate and cobalt dihydride complex, which are involved in the subsequent reductive amination. This strategy provides a green and effective route for alcohol amination, which may have promising applications in alcohol-involved alkylation reactions." @default.
- W4376642780 created "2023-05-17" @default.
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- W4376642780 date "2023-07-10" @default.
- W4376642780 modified "2023-10-17" @default.
- W4376642780 title "Ionic‐Liquid Hydrogen‐Bonding Promoted Alcohols Amination over Cobalt Catalyst via Dihydrogen Autotransfer Mechanism" @default.
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- W4376642780 doi "https://doi.org/10.1002/cssc.202300513" @default.
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- W4376642780 hasPublicationYear "2023" @default.
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