Synthesis of novel quinolines using TsOH/ionic liquid under microwave
Autor(a) principal: | |
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Data de Publicação: | 2012 |
Outros Autores: | , , , , , , , |
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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Journal of the Brazilian Chemical Society (Online) |
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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 |
_version_ |
1750318174075617280 |