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Room Temperature Aerobic Copper–Catalysed Selective Oxidation of Primary Alcohols to Aldehydes
Author(s) -
Gamez Patrick,
Arends Isabel W. C. E.,
Sheldon Roger A.,
Reedijk Jan
Publication year - 2004
Publication title -
advanced synthesis and catalysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.541
H-Index - 155
eISSN - 1615-4169
pISSN - 1615-4150
DOI - 10.1002/adsc.200404063
Subject(s) - chemistry , galactose oxidase , acetonitrile , catalysis , alcohol oxidation , copper , solvent , salt (chemistry) , ligand (biochemistry) , inorganic chemistry , primary (astronomy) , photochemistry , polymer chemistry , organic chemistry , galactose , biochemistry , physics , receptor , astronomy
A novel and very mild method for the oxidation of primary alcohols to aldehydes with excellent conversions has been developed. The reaction is carried out under air at room temperature and is catalysed using a [copper(II)‐(N ligand) n ] complex with TEMPO and a base as co‐catalysts. In this paper, the performance of a series of N‐containing ligands, as well as different copper(II) salt precursors in different solvents are reported. Best results are obtained in acetonitrile/water as solvent using a copper(II) catalyst generated in situ from a Cu(II) salt with weak or non‐coordinating anions and bipyridine ligands with electron‐donating substituents. A reaction mechanism is postulated which resembles that of galactose oxidase, and in which TEMPO seems to be involved as a hydrogen acceptor.