Síntese de 3-alcoxiacrilamidas a partir de tricloroacetil enol éteres

Detalhes bibliográficos
Autor(a) principal: Mello, Débora Lombe de
Data de Publicação: 2012
Tipo de documento: Dissertação
Idioma: por
Título da fonte: Manancial - Repositório Digital da UFSM
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
id UFSM_173a7c41f2115c859e9cec1e618aa9c5
oai_identifier_str oai:repositorio.ufsm.br:1/10518
network_acronym_str UFSM
network_name_str Manancial - Repositório Digital da UFSM
repository_id_str
spelling 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/1/10518porinfo: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
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.
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_ 1805922033979097088