Síntese de 3-alcoxiacrilamidas a partir de tricloroacetil enol éteres

Detalhes bibliográficos
Ano de defesa: 2012
Autor(a) principal: Mello, Débora Lombe de lattes
Orientador(a): Zanatta, Nilo lattes
Banca de defesa: Flores, Alex Fabiani Claro lattes, Fantinel, Leonardo lattes
Tipo de documento: Dissertação
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Federal de Santa Maria
Programa de Pós-Graduação: Programa de Pós-Graduação em Química
Departamento: Química
País: BR
Palavras-chave em Português:
Palavras-chave em Inglês:
Área do conhecimento CNPq:
Link de acesso: 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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spelling 2017-05-122017-05-122012-02-24MELLO, 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/1/10518This 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.application/pdfporUniversidade Federal de Santa MariaPrograma de Pós-Graduação em QuímicaUFSMBRQuímica3-alcoxiacrilamidasÁcidos β-alcoxivinil carboxílicosβ-alcoxivinil tricloroacetil cetonasCloretos ácidosAminas primárias alquílicas3-alkoxy acrylamidesβ-alkoxyvinyl carboxylic acidsβ-alkoxyvinyl trichloroacetyl ketonesAcyl chloridesAminesCNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICASíntese de 3-alcoxiacrilamidas a partir de tricloroacetil enol éteresSynthesis of 3-alkoxy acrylamides from trichloroacetil enol ethersinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisZanatta, Nilohttp://lattes.cnpq.br/0719465062354576Flores, Alex Fabiani Clarohttp://lattes.cnpq.br/1159954352174167Fantinel, Leonardohttp://lattes.cnpq.br/3934644027018397http://lattes.cnpq.br/0395675025653002Mello, Débora Lombe de100600000000400500300500500233dc1de-ab03-4f57-9b85-e40dc01a2d4f70386445-7f10-464a-be01-fc2355abd7f74d308e51-3866-4274-9e77-03644c9383df079f4612-cd36-4354-af6f-25f7736dccd2info:eu-repo/semantics/openAccessreponame:Manancial - Repositório Digital da UFSMinstname:Universidade Federal de Santa Maria (UFSM)instacron:UFSMORIGINALMELLO, DEBORA LOMBE DE.pdfapplication/pdf4372333http://repositorio.ufsm.br/bitstream/1/10518/1/MELLO%2c%20DEBORA%20LOMBE%20DE.pdfcdabf27c076b067c6b562543a075756dMD51TEXTMELLO, DEBORA LOMBE DE.pdf.txtMELLO, DEBORA LOMBE DE.pdf.txtExtracted texttext/plain137193http://repositorio.ufsm.br/bitstream/1/10518/2/MELLO%2c%20DEBORA%20LOMBE%20DE.pdf.txt87e8452097c02c3a2f77fffa30be7f3aMD52THUMBNAILMELLO, DEBORA LOMBE DE.pdf.jpgMELLO, DEBORA LOMBE DE.pdf.jpgIM Thumbnailimage/jpeg5733http://repositorio.ufsm.br/bitstream/1/10518/3/MELLO%2c%20DEBORA%20LOMBE%20DE.pdf.jpg828e5e639fbfab6930bc82e1d8dd7200MD531/105182023-06-14 12:31:08.252oai:repositorio.ufsm.br:1/10518Repositório Institucionalhttp://repositorio.ufsm.br/PUBhttp://repositorio.ufsm.br/oai/requestopendoar:39132023-06-14T15:31:08Manancial - Repositório Digital da UFSM - Universidade Federal de Santa Maria (UFSM)false
dc.title.por.fl_str_mv Síntese de 3-alcoxiacrilamidas a partir de tricloroacetil enol éteres
dc.title.alternative.eng.fl_str_mv 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.advisor1.fl_str_mv Zanatta, Nilo
dc.contributor.advisor1Lattes.fl_str_mv http://lattes.cnpq.br/0719465062354576
dc.contributor.referee1.fl_str_mv Flores, Alex Fabiani Claro
dc.contributor.referee1Lattes.fl_str_mv http://lattes.cnpq.br/1159954352174167
dc.contributor.referee2.fl_str_mv Fantinel, Leonardo
dc.contributor.referee2Lattes.fl_str_mv http://lattes.cnpq.br/3934644027018397
dc.contributor.authorLattes.fl_str_mv http://lattes.cnpq.br/0395675025653002
dc.contributor.author.fl_str_mv Mello, Débora Lombe de
contributor_str_mv Zanatta, Nilo
Flores, Alex Fabiani Claro
Fantinel, Leonardo
dc.subject.por.fl_str_mv 3-alcoxiacrilamidas
Ácidos β-alcoxivinil carboxílicos
β-alcoxivinil tricloroacetil cetonas
Cloretos ácidos
Aminas primárias alquílicas
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
dc.subject.eng.fl_str_mv 3-alkoxy acrylamides
β-alkoxyvinyl carboxylic acids
β-alkoxyvinyl trichloroacetyl ketones
Acyl chlorides
Amines
dc.subject.cnpq.fl_str_mv 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.issued.fl_str_mv 2012-02-24
dc.date.accessioned.fl_str_mv 2017-05-12
dc.date.available.fl_str_mv 2017-05-12
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dc.identifier.citation.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.
dc.identifier.uri.fl_str_mv 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
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dc.publisher.department.fl_str_mv Química
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