Clean preparation of methyl esters in one-step oxidative esterification of primary alcohols catalyzed by supported gold nanoparticles


Autoria(s): Oliveira, Rafael de Lima; Kiyohara, Pedro Kunihiko; Rossi, Liane Marcia
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

18/04/2012

18/04/2012

2009

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

http://dx.doi.org/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