The alkylation of arylamines using stoichiometric amounts of aliphatic and benzylic alcohols in the presence of tBuOK was carried out at 55 °C using a low catalyst loading of [Ru(cod)Cl2]n/PTA (1,3,5-triaza-7-phosphaadamantane). The overall borrowing-hydrogen process does not require a controlled nitrogen atmosphere, and it could also be carried out at room temperature using higher loading of base. A wide range of substrates can be used in this transformation, and it has a good tolerance of different substituents. This catalytic system proved also to be efficient for other hydrogen-transfer reactions such as a tandem oxidation/C-C coupling between 1-phenylethanol and primary alcohols.

A Ruthenium-Based Catalytic System for a Mild Borrowing-Hydrogen Process

Gonsalvi, Luca;Guerriero, Antonella;Peruzzini, Maurizio;Taddei, Maurizio
2015

Abstract

The alkylation of arylamines using stoichiometric amounts of aliphatic and benzylic alcohols in the presence of tBuOK was carried out at 55 °C using a low catalyst loading of [Ru(cod)Cl2]n/PTA (1,3,5-triaza-7-phosphaadamantane). The overall borrowing-hydrogen process does not require a controlled nitrogen atmosphere, and it could also be carried out at room temperature using higher loading of base. A wide range of substrates can be used in this transformation, and it has a good tolerance of different substituents. This catalytic system proved also to be efficient for other hydrogen-transfer reactions such as a tandem oxidation/C-C coupling between 1-phenylethanol and primary alcohols.
2015
Istituto di Chimica dei Composti OrganoMetallici - ICCOM -
Inglese
8
1829
1833
5
https://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/ejoc.201403636
Esperti anonimi
Alcohols
Alkylation
Amines
Homogeneous catalysis
Hydrogen transfer
Ruthenium
Elettronico
5
info:eu-repo/semantics/article
262
Jumde, Varsha R.; Gonsalvi, Luca; Guerriero, Antonella; Peruzzini, Maurizio; Taddei, Maurizio
01 Contributo su Rivista::01.01 Articolo in rivista
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/319565
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