Synthesis of novel quinolines using TsOH/ionic liquid under microwave

Detalhes bibliográficos
Autor(a) principal: Prola,Liziê D. T.
Data de Publicação: 2012
Outros Autores: Buriol,Lilian, Frizzo,Clarissa P., Caleffi,Guilherme S., Marzari,Mara R. B., Moreira,Dayse N., Bonacorso,Helio G., Zanatta,Nilo, Martins,Marcos A. P.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Journal of the Brazilian Chemical Society (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532012000900011
Resumo: In this work, 3-haloacetyl-4-methylquinolines were synthesized from the reaction of 4-alkoxy-3-alken-2-ones [R¹C(O)CH=C(R²)OCH3, where R¹ = CF3, CCl3, CHCl2, CF2Cl, CF2CF3 and R² = Me, Et, Pr, Bu, i-Bu and i-Pe] and 2-aminoacetophenone. The reaction was performed in ionic liquid and 4-toluene sulfonic acid under microwave irradiation. Results showed that the catalytic method was effective. Products were formed in a short time (10-20 min) and presented good yields (70-91%).
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spelling Synthesis of novel quinolines using TsOH/ionic liquid under microwaveionic liquidquinolinetoluene sulfonic acidmicrowave-assisted synthesis (MW)enonesIn this work, 3-haloacetyl-4-methylquinolines were synthesized from the reaction of 4-alkoxy-3-alken-2-ones [R¹C(O)CH=C(R²)OCH3, where R¹ = CF3, CCl3, CHCl2, CF2Cl, CF2CF3 and R² = Me, Et, Pr, Bu, i-Bu and i-Pe] and 2-aminoacetophenone. The reaction was performed in ionic liquid and 4-toluene sulfonic acid under microwave irradiation. Results showed that the catalytic method was effective. Products were formed in a short time (10-20 min) and presented good yields (70-91%).Sociedade Brasileira de Química2012-09-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532012000900011Journal of the Brazilian Chemical Society v.23 n.9 2012reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532012005000030info:eu-repo/semantics/openAccessProla,Liziê D. T.Buriol,LilianFrizzo,Clarissa P.Caleffi,Guilherme S.Marzari,Mara R. B.Moreira,Dayse N.Bonacorso,Helio G.Zanatta,NiloMartins,Marcos A. P.eng2012-10-15T00:00:00Zoai:scielo:S0103-50532012000900011Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2012-10-15T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Synthesis of novel quinolines using TsOH/ionic liquid under microwave
title Synthesis of novel quinolines using TsOH/ionic liquid under microwave
spellingShingle Synthesis of novel quinolines using TsOH/ionic liquid under microwave
Prola,Liziê D. T.
ionic liquid
quinoline
toluene sulfonic acid
microwave-assisted synthesis (MW)
enones
title_short Synthesis of novel quinolines using TsOH/ionic liquid under microwave
title_full Synthesis of novel quinolines using TsOH/ionic liquid under microwave
title_fullStr Synthesis of novel quinolines using TsOH/ionic liquid under microwave
title_full_unstemmed Synthesis of novel quinolines using TsOH/ionic liquid under microwave
title_sort Synthesis of novel quinolines using TsOH/ionic liquid under microwave
author Prola,Liziê D. T.
author_facet Prola,Liziê D. T.
Buriol,Lilian
Frizzo,Clarissa P.
Caleffi,Guilherme S.
Marzari,Mara R. B.
Moreira,Dayse N.
Bonacorso,Helio G.
Zanatta,Nilo
Martins,Marcos A. P.
author_role author
author2 Buriol,Lilian
Frizzo,Clarissa P.
Caleffi,Guilherme S.
Marzari,Mara R. B.
Moreira,Dayse N.
Bonacorso,Helio G.
Zanatta,Nilo
Martins,Marcos A. P.
author2_role author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Prola,Liziê D. T.
Buriol,Lilian
Frizzo,Clarissa P.
Caleffi,Guilherme S.
Marzari,Mara R. B.
Moreira,Dayse N.
Bonacorso,Helio G.
Zanatta,Nilo
Martins,Marcos A. P.
dc.subject.por.fl_str_mv ionic liquid
quinoline
toluene sulfonic acid
microwave-assisted synthesis (MW)
enones
topic ionic liquid
quinoline
toluene sulfonic acid
microwave-assisted synthesis (MW)
enones
description In this work, 3-haloacetyl-4-methylquinolines were synthesized from the reaction of 4-alkoxy-3-alken-2-ones [R¹C(O)CH=C(R²)OCH3, where R¹ = CF3, CCl3, CHCl2, CF2Cl, CF2CF3 and R² = Me, Et, Pr, Bu, i-Bu and i-Pe] and 2-aminoacetophenone. The reaction was performed in ionic liquid and 4-toluene sulfonic acid under microwave irradiation. Results showed that the catalytic method was effective. Products were formed in a short time (10-20 min) and presented good yields (70-91%).
publishDate 2012
dc.date.none.fl_str_mv 2012-09-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532012000900011
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532012000900011
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0103-50532012005000030
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Brasileira de Química
publisher.none.fl_str_mv Sociedade Brasileira de Química
dc.source.none.fl_str_mv Journal of the Brazilian Chemical Society v.23 n.9 2012
reponame:Journal of the Brazilian Chemical Society (Online)
instname:Sociedade Brasileira de Química (SBQ)
instacron:SBQ
instname_str Sociedade Brasileira de Química (SBQ)
instacron_str SBQ
institution SBQ
reponame_str Journal of the Brazilian Chemical Society (Online)
collection Journal of the Brazilian Chemical Society (Online)
repository.name.fl_str_mv Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)
repository.mail.fl_str_mv ||office@jbcs.sbq.org.br
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