Clean preparation of methyl esters in one-step oxidative esterification of primary alcohols catalyzed by supported gold nanoparticles
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
18/04/2012
18/04/2012
2009
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Resumo |
Methyl esters were prepared by the clean, one-step catalytic esterification of primary alcohols using molecular oxygen as a green oxidant and a newly developed SiO(2)-supported gold nanoparticle catalyst. The catalyst was highly active and selective in a broad range of pressure and temperature. At 3 atm O(2) and 130 degrees C benzyl alcohol was converted to methyl benzoate with 100% conversion and 100% selectivity in 4 h of reaction. This catalytic process is much ""greener"" than the conventional reaction routes because it avoids the use of stoichiometric environmentally unfriendly oxidants, usually required for alcohol oxidation, and the use of strong acids or excess of reactants or constant removal of products required to shift the equilibrium to the desired esterification product. FAPESP CNPq |
Identificador |
GREEN CHEMISTRY, v.11, n.9, p.1366-1370, 2009 1463-9262 http://producao.usp.br/handle/BDPI/16104 10.1039/b902499a |
Idioma(s) |
eng |
Publicador |
ROYAL SOC CHEMISTRY |
Relação |
Green Chemistry |
Direitos |
closedAccess Copyright ROYAL SOC CHEMISTRY |
Palavras-Chave | #AEROBIC OXIDATION #SELECTIVE OXIDATION #MOLECULAR-OXYGEN #METAL-OXIDES #ALDEHYDES #TRANSFORMATION #NANOCLUSTERS #EPOXIDATION #STYRENE #FACILE #Chemistry, Multidisciplinary |
Tipo |
article original article publishedVersion |