dc.creatorCardoso, Luiz Augusto Martins
dc.creatorAlves Junior, Walter
dc.creatorGonzaga, Angélica Raimunda Esquerdo
dc.creatorAguiar, Leila Maria Guimaraes
dc.creatorAndrade, Heloysa Martins Carvalho
dc.creatorCardoso, Luiz Augusto Martins
dc.creatorAlves Junior, Walter
dc.creatorGonzaga, Angélica Raimunda Esquerdo
dc.creatorAguiar, Leila Maria Guimaraes
dc.creatorAndrade, Heloysa Martins Carvalho
dc.date.accessioned2022-10-07T16:06:35Z
dc.date.available2022-10-07T16:06:35Z
dc.date.issued2004
dc.identifier1381-1169
dc.identifierhttp://www.repositorio.ufba.br/ri/handle/ri/7915
dc.identifierv. 209, n. 1-2
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/4006660
dc.description.abstractMethoxyacetophenones were synthesized through Friedel–Crafts acylation of anisole with acetic anhydride using a silica-supported heteropolyphosphotungstic acid (HPW) catalyst. High conversions and very high p-selectivity were attained in the temperature range of 61–110 °C.Nevertheless, the catalyst seemed to deactivate after half an hour at 61 and 83 °C, mainly due to strong but reversible adsorption of products. Cleaning the spent catalyst recovered the activity, indicating that it was stable under the experimental conditions and that the active HPW was not fairly leached from the silica support. In spite of this, the slower but progressive coking deactivated the catalyst.
dc.languageen
dc.publisherElservier
dc.sourcehttp://dx.doi.org/10.1016/j.molcata.2003.08.022
dc.subjectFriedel–Crafts acylation
dc.subjectMethoxyacetophenones
dc.subjectHeteropolyacids
dc.subjectAcid anhydride
dc.subjectAnisole
dc.titleFriedel–Crafts acylation of anisole with acetic anhydride over silica-supported heteropolyphosphotungstic acid (HPW/SiO2)
dc.typeArtigo Publicado em Periódico


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