Síntese de 3-alcoxiacrilamidas a partir de tricloroacetil enol éteres
Autor(a) principal: | |
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Data de Publicação: | 2012 |
Tipo de documento: | Dissertação |
Idioma: | por |
Título da fonte: | Manancial - Repositório Digital da UFSM |
dARK ID: | ark:/26339/0013000004kgz |
Texto Completo: | http://repositorio.ufsm.br/handle/1/10518 |
Resumo: | This work reports a effective method for the preparation of a series of the new 3-alkoxy acrylamides of general formula R3HNC(O)CR1=CR2(OR), where R/ R1/ R2 = Et/H/H, Me/H/Me, -(CH2)2-/H, -(CH2)3-/H; R3 = Allyl, n-Pr, Bn, Phenetyl. However, the 3-alkoxy acrylamides where R/ R1/ R2 = Et/H/H/, Me/H/Me, R3 = Bn, have already been described in the literature. The 3-alkoxy acrylamides were obtained through three reaction steps. The first step, β-alkoxyvinyl trichloroacetyl ketones were synthesized through the acylation of enolethers using trichloroacetyl chloride as the acylating agent. In the second step, β-alkoxyvinyl trichloroacetyl ketones were converted to the corresponding β-alkoxyvinyl carboxylic acids from a basic hydrolysis using a 1 M sodium hydroxide solution. In the third step, β-alkoxyvinyl carboxylic acids were treated with thionyl chloride, using toluene as solvent, leading to the corresponding acyl chlorides intermediaries, which were not isolated. The acyl chlorides were reacted with primary amines such as allylamine, propylamine, benzylamine, and phenethylamine under basic catalysis of triethylamine, furnishing a new series of 3-alkoxy acrylamides in good yields of 48-90%. The 3-alkoxy acrylamides obtained in this study were identified by 1H and 13C Nuclear Magnetic Resonance spectroscopy, Mass spectroscopy and Elemental analysis. Keywords: 3-alkoxy acrylamides, β-alkoxyvinyl carboxylic acids, β-alkoxyvinyl trichloroacetyl ketones, acyl chlorides, amines |
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Síntese de 3-alcoxiacrilamidas a partir de tricloroacetil enol éteresSynthesis of 3-alkoxy acrylamides from trichloroacetil enol ethers3-alcoxiacrilamidasÁcidos β-alcoxivinil carboxílicosβ-alcoxivinil tricloroacetil cetonasCloretos ácidosAminas primárias alquílicas3-alkoxy acrylamidesβ-alkoxyvinyl carboxylic acidsβ-alkoxyvinyl trichloroacetyl ketonesAcyl chloridesAminesCNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICAThis work reports a effective method for the preparation of a series of the new 3-alkoxy acrylamides of general formula R3HNC(O)CR1=CR2(OR), where R/ R1/ R2 = Et/H/H, Me/H/Me, -(CH2)2-/H, -(CH2)3-/H; R3 = Allyl, n-Pr, Bn, Phenetyl. However, the 3-alkoxy acrylamides where R/ R1/ R2 = Et/H/H/, Me/H/Me, R3 = Bn, have already been described in the literature. The 3-alkoxy acrylamides were obtained through three reaction steps. The first step, β-alkoxyvinyl trichloroacetyl ketones were synthesized through the acylation of enolethers using trichloroacetyl chloride as the acylating agent. In the second step, β-alkoxyvinyl trichloroacetyl ketones were converted to the corresponding β-alkoxyvinyl carboxylic acids from a basic hydrolysis using a 1 M sodium hydroxide solution. In the third step, β-alkoxyvinyl carboxylic acids were treated with thionyl chloride, using toluene as solvent, leading to the corresponding acyl chlorides intermediaries, which were not isolated. The acyl chlorides were reacted with primary amines such as allylamine, propylamine, benzylamine, and phenethylamine under basic catalysis of triethylamine, furnishing a new series of 3-alkoxy acrylamides in good yields of 48-90%. The 3-alkoxy acrylamides obtained in this study were identified by 1H and 13C Nuclear Magnetic Resonance spectroscopy, Mass spectroscopy and Elemental analysis. Keywords: 3-alkoxy acrylamides, β-alkoxyvinyl carboxylic acids, β-alkoxyvinyl trichloroacetyl ketones, acyl chlorides, aminesEste trabalho apresenta um método eficiente para preparação de uma série inédita de 3-alcoxiacrilamidas de fórmula geral R3HNC(O)CR1=CR2(OR), onde R/ R1/R2 = Et/H/H, Me/H/Me, -(CH2)2-/H, -(CH2)3-/H; R3 = Alil, n-Pr, Bn, Fenetil. Sendo que as 3-alcoxiacrilamidas onde R/ R1/ R2 = Et/H/H, Me/H/Me, R3 = Bn, já foram descritas anteriormente na literatura. As 3-alcoxiacrilamidas foram obtidas através de três etapas reacionais, sendo que a primeira etapa constitui-se da acilação dos enol éteres, utilizando cloreto de tricloroacetila como agente acilante. Na segunda etapa as β-alcoxivinil tricloroacetil cetonas sintetizadas anteriormente, foram convertidas aos respectivos ácidos β-alcoxivinil carboxílicos a partir da hidrólise básica (utilizando solução de NaOH 1 M). Na terceira etapa, os ácidos β-alcoxivinil carboxílicos foram submetidos à reação com cloreto de tionila, utilizando tolueno como solvente, formando como intermediários os cloretos ácidos, os quais não foram isolados. Posteriormente, esses cloretos ácidos foram submetidos á reação de substituição nucleofílica, utilizando diferentes aminas alquílicas primárias (alilamina, propilamina, benzilamina, fenetilamina) como nucleófilo, sob catálise básica de trietilamina, promovendo assim, a síntese da série inédita das 3-alcoxiacrilamidas com bons rendimentos de 48-90%. As 3-alcoxiacrilamidas obtidas neste trabalho foram identificadas através de técnicas de Ressonância Magnética Nuclear de Hidrogênio, Ressonância Magnética Nuclear de Carbono-13, Espectrometria de Massas e Análise elementar.Universidade Federal de Santa MariaBRQuímicaUFSMPrograma de Pós-Graduação em QuímicaZanatta, Nilohttp://lattes.cnpq.br/0719465062354576Flores, Alex Fabiani Clarohttp://lattes.cnpq.br/1159954352174167Fantinel, Leonardohttp://lattes.cnpq.br/3934644027018397Mello, Débora Lombe de2017-05-122017-05-122012-02-24info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisapplication/pdfapplication/pdfMELLO, Débora Lombe de. Synthesis of 3-alkoxy acrylamides from trichloroacetil enol ethers. 2012. 125 f. Dissertação (Mestrado em Química) - Universidade Federal de Santa Maria, Santa Maria, 2012.http://repositorio.ufsm.br/handle/1/10518ark:/26339/0013000004kgzporinfo:eu-repo/semantics/openAccessreponame:Manancial - Repositório Digital da UFSMinstname:Universidade Federal de Santa Maria (UFSM)instacron:UFSM2023-06-14T15:31:08Zoai:repositorio.ufsm.br:1/10518Biblioteca Digital de Teses e Dissertaçõeshttps://repositorio.ufsm.br/ONGhttps://repositorio.ufsm.br/oai/requestatendimento.sib@ufsm.br||tedebc@gmail.comopendoar:2023-06-14T15:31:08Manancial - Repositório Digital da UFSM - Universidade Federal de Santa Maria (UFSM)false |
dc.title.none.fl_str_mv |
Síntese de 3-alcoxiacrilamidas a partir de tricloroacetil enol éteres Synthesis of 3-alkoxy acrylamides from trichloroacetil enol ethers |
title |
Síntese de 3-alcoxiacrilamidas a partir de tricloroacetil enol éteres |
spellingShingle |
Síntese de 3-alcoxiacrilamidas a partir de tricloroacetil enol éteres Mello, Débora Lombe de 3-alcoxiacrilamidas Ácidos β-alcoxivinil carboxílicos β-alcoxivinil tricloroacetil cetonas Cloretos ácidos Aminas primárias alquílicas 3-alkoxy acrylamides β-alkoxyvinyl carboxylic acids β-alkoxyvinyl trichloroacetyl ketones Acyl chlorides Amines CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA |
title_short |
Síntese de 3-alcoxiacrilamidas a partir de tricloroacetil enol éteres |
title_full |
Síntese de 3-alcoxiacrilamidas a partir de tricloroacetil enol éteres |
title_fullStr |
Síntese de 3-alcoxiacrilamidas a partir de tricloroacetil enol éteres |
title_full_unstemmed |
Síntese de 3-alcoxiacrilamidas a partir de tricloroacetil enol éteres |
title_sort |
Síntese de 3-alcoxiacrilamidas a partir de tricloroacetil enol éteres |
author |
Mello, Débora Lombe de |
author_facet |
Mello, Débora Lombe de |
author_role |
author |
dc.contributor.none.fl_str_mv |
Zanatta, Nilo http://lattes.cnpq.br/0719465062354576 Flores, Alex Fabiani Claro http://lattes.cnpq.br/1159954352174167 Fantinel, Leonardo http://lattes.cnpq.br/3934644027018397 |
dc.contributor.author.fl_str_mv |
Mello, Débora Lombe de |
dc.subject.por.fl_str_mv |
3-alcoxiacrilamidas Ácidos β-alcoxivinil carboxílicos β-alcoxivinil tricloroacetil cetonas Cloretos ácidos Aminas primárias alquílicas 3-alkoxy acrylamides β-alkoxyvinyl carboxylic acids β-alkoxyvinyl trichloroacetyl ketones Acyl chlorides Amines CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA |
topic |
3-alcoxiacrilamidas Ácidos β-alcoxivinil carboxílicos β-alcoxivinil tricloroacetil cetonas Cloretos ácidos Aminas primárias alquílicas 3-alkoxy acrylamides β-alkoxyvinyl carboxylic acids β-alkoxyvinyl trichloroacetyl ketones Acyl chlorides Amines CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA |
description |
This work reports a effective method for the preparation of a series of the new 3-alkoxy acrylamides of general formula R3HNC(O)CR1=CR2(OR), where R/ R1/ R2 = Et/H/H, Me/H/Me, -(CH2)2-/H, -(CH2)3-/H; R3 = Allyl, n-Pr, Bn, Phenetyl. However, the 3-alkoxy acrylamides where R/ R1/ R2 = Et/H/H/, Me/H/Me, R3 = Bn, have already been described in the literature. The 3-alkoxy acrylamides were obtained through three reaction steps. The first step, β-alkoxyvinyl trichloroacetyl ketones were synthesized through the acylation of enolethers using trichloroacetyl chloride as the acylating agent. In the second step, β-alkoxyvinyl trichloroacetyl ketones were converted to the corresponding β-alkoxyvinyl carboxylic acids from a basic hydrolysis using a 1 M sodium hydroxide solution. In the third step, β-alkoxyvinyl carboxylic acids were treated with thionyl chloride, using toluene as solvent, leading to the corresponding acyl chlorides intermediaries, which were not isolated. The acyl chlorides were reacted with primary amines such as allylamine, propylamine, benzylamine, and phenethylamine under basic catalysis of triethylamine, furnishing a new series of 3-alkoxy acrylamides in good yields of 48-90%. The 3-alkoxy acrylamides obtained in this study were identified by 1H and 13C Nuclear Magnetic Resonance spectroscopy, Mass spectroscopy and Elemental analysis. Keywords: 3-alkoxy acrylamides, β-alkoxyvinyl carboxylic acids, β-alkoxyvinyl trichloroacetyl ketones, acyl chlorides, amines |
publishDate |
2012 |
dc.date.none.fl_str_mv |
2012-02-24 2017-05-12 2017-05-12 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/masterThesis |
format |
masterThesis |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
MELLO, Débora Lombe de. Synthesis of 3-alkoxy acrylamides from trichloroacetil enol ethers. 2012. 125 f. Dissertação (Mestrado em Química) - Universidade Federal de Santa Maria, Santa Maria, 2012. http://repositorio.ufsm.br/handle/1/10518 |
dc.identifier.dark.fl_str_mv |
ark:/26339/0013000004kgz |
identifier_str_mv |
MELLO, Débora Lombe de. Synthesis of 3-alkoxy acrylamides from trichloroacetil enol ethers. 2012. 125 f. Dissertação (Mestrado em Química) - Universidade Federal de Santa Maria, Santa Maria, 2012. ark:/26339/0013000004kgz |
url |
http://repositorio.ufsm.br/handle/1/10518 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
Universidade Federal de Santa Maria BR Química UFSM Programa de Pós-Graduação em Química |
publisher.none.fl_str_mv |
Universidade Federal de Santa Maria BR Química UFSM Programa de Pós-Graduação em Química |
dc.source.none.fl_str_mv |
reponame:Manancial - Repositório Digital da UFSM instname:Universidade Federal de Santa Maria (UFSM) instacron:UFSM |
instname_str |
Universidade Federal de Santa Maria (UFSM) |
instacron_str |
UFSM |
institution |
UFSM |
reponame_str |
Manancial - Repositório Digital da UFSM |
collection |
Manancial - Repositório Digital da UFSM |
repository.name.fl_str_mv |
Manancial - Repositório Digital da UFSM - Universidade Federal de Santa Maria (UFSM) |
repository.mail.fl_str_mv |
atendimento.sib@ufsm.br||tedebc@gmail.com |
_version_ |
1815172282104938496 |