Deep eutectic solvents as H2-sources for Ru(II)-catalyzed transfer hydrogenation of carbonyl compounds under mild conditions

被引:20
|
作者
Cavallo, Marzia [1 ]
Arnodo, Davide [1 ]
Mannu, Alberto [1 ]
Blangetti, Marco [1 ]
Prandi, Cristina [1 ]
Baratta, Walter [2 ]
Baldino, Salvatore [1 ]
机构
[1] Dipartimento Chim, Via P Giuria 7, I-10125 Turin, Italy
[2] Univ Udine, Dipartimento DI4A, Via Cotonificio 108, I-33100 Udine, Italy
关键词
Deep eutectic solvents; Ruthenium; Ligands; Carbonyl compounds; Transfer hydrogenation;
D O I
10.1016/j.tet.2021.131997
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The employment of easily affordable ruthenium(II)-complexes as pre-catalysts in the transfer hydrogenation of carbonyl compounds in deep eutectic media is described for the first time. The eutectic mixture tetrabutylammonium bromide/formic acid = 1/1 (TBABr/HCOOH = 1/1) acts both as reaction medium and hydrogen source. The addition of a base is required for the process to occur. An extensive optimization of the reaction conditions has been carried out, in terms of catalyst loading, type of complexes, H-2-donors, reaction temperature and time. The combination of the dimeric complex [RuCl(p-cymene)-mu-Cl](2) (0.01-0.05 eq.) and the ligand dppf (1,10-ferrocenediyl-bis(diphenylphosphine)ferrocene) in 1/1 molar ratio has proven to be a suitable catalytic system for the reduction of several and diverse aldehydes and ketones to their corresponding alcohols under mild conditions (40-60 degrees C) in air, showing from moderate to excellent tolerability towards different functional groups (halogen, cyano, nitro, phenol). The reduction of imine compounds to their corresponding amine derivatives was also studied. In addition, the comparison between the results obtained in TBABr/HCOOH and in organic solvents suggests a non-innocent effect of the DES medium during the process. (C) 2021 Elsevier Ltd. All rights reserved.
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页数:11
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