Síntese de compostos heteroazóicos substituídos no solvente alternativo PEG 400
| Ano de defesa: | 2018 |
|---|---|
| Autor(a) principal: | |
| Orientador(a): | |
| Banca de defesa: | , , , |
| Tipo de documento: | Dissertação |
| Tipo de acesso: | Acesso aberto |
| dARK ID: | ark:/38995/0013000005t8t |
| Idioma: | por |
| Instituição de defesa: |
Universidade Federal de Goiás
|
| Programa de Pós-Graduação: |
Programa de Pós-graduação em Química (IQ)
|
| Departamento: |
Instituto de Química - IQ (RG)
|
| País: |
Brasil
|
| Palavras-chave em Português: | |
| Palavras-chave em Inglês: | |
| Área do conhecimento CNPq: | |
| Link de acesso: | http://repositorio.bc.ufg.br/tede/handle/tede/8679 |
Resumo: | The present work describes the development of a simple and efficient methodology for the synthesis of 2-aminoheteroazoic compounds using the solvent PEG 400 as an alternative to toxic and flammable organic solvents. Several media and reactional conditions were compared. A series of substituted 2-aminothiazoic compounds was obtained in good yields (60 to 96%) by a 3 hour reaction procedure using PEG 400 at room temperature and without the need for additives or catalysts. A selenium analogue and a 2-imino-1,3-thiazoline were also obtained by this method. The products were characterized by 1H and 13C NMR and infrared spectroscopies and mass spectrometry. The method covers some points of Green Chemistry, such as: safe synthesis, prevention in the formation of residues or derivatives, development of products that do not harm the environment, energy efficiency and accident prevention. |
| id |
UFG-2_9a58d01e02df085b15fc02a709cebf8a |
|---|---|
| oai_identifier_str |
oai:repositorio.bc.ufg.br:tede/8679 |
| network_acronym_str |
UFG-2 |
| network_name_str |
Repositório Institucional da UFG |
| repository_id_str |
|
| spelling |
Barros, Olga Soares do Rêgohttp://lattes.cnpq.br/8311808341863723Chagas, Rafael Pavão dashttp://lattes.cnpq.br/9712618482518275Barros, Olga Soares do Rêgohttp://lattes.cnpq.br/8311808341863723Chagas, Rafael Pavão dasMilani, Jorge Luiz SônegoCosta, Maisa Borgeshttp://lattes.cnpq.br/7794429925120494Ferreira, Achiles Silva2018-07-11T10:40:15Z2018-04-27FERREIRA, A. S. Síntese de compostos heteroazóicos substituídos no solvente alternativo PEG 400. 2018. 76 f. Dissertação (Mestrado em Química) - Universidade Federal de Goiás, Goiânia, 2018.http://repositorio.bc.ufg.br/tede/handle/tede/8679ark:/38995/0013000005t8tThe present work describes the development of a simple and efficient methodology for the synthesis of 2-aminoheteroazoic compounds using the solvent PEG 400 as an alternative to toxic and flammable organic solvents. Several media and reactional conditions were compared. A series of substituted 2-aminothiazoic compounds was obtained in good yields (60 to 96%) by a 3 hour reaction procedure using PEG 400 at room temperature and without the need for additives or catalysts. A selenium analogue and a 2-imino-1,3-thiazoline were also obtained by this method. The products were characterized by 1H and 13C NMR and infrared spectroscopies and mass spectrometry. The method covers some points of Green Chemistry, such as: safe synthesis, prevention in the formation of residues or derivatives, development of products that do not harm the environment, energy efficiency and accident prevention.O presente trabalho descreve o desenvolvimento de uma metodologia simples e eficiente para a síntese de compostos 2-amino-heteroazóicos, utilizando o solvente PEG 400 como alternativa a solventes orgânicos tóxicos e inflamáveis. Diversos meios e condições reacionais foram comparados. Uma série de compostos 2-amino-tioazóicos substituídos foi obtida, em bons rendimentos (60 a 96%), através de procedimento reacional com 3 horas de duração, utilizando PEG 400 à temperatura ambiente e sem a necessidade de aditivos ou catalisadores. Um análogo de selênio e uma 2-imino-1,3-tiazolina também foram obtidos através desse método. Os produtos foram caracterizados por espectroscopias de RMN de 1H e 13C e infravermelho e espectrometria de massas. O método abrange alguns pontos da Química Verde, como: síntese segura, prevenção na formação de resíduos ou derivados, desenvolvimento de produtos que não agridem o meio ambiente, eficiência energética e prevenção de acidentes.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPESapplication/pdfporUniversidade Federal de GoiásPrograma de Pós-graduação em Química (IQ)UFGBrasilInstituto de Química - IQ (RG)http://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/openAccessSínteseHeterocíclicosSynthesisHeterocyclicsQUIMICA::QUIMICA ORGANICASíntese de compostos heteroazóicos substituídos no solvente alternativo PEG 400Synthesis of heteroazo compounds in alternative solvent PEG 400info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesis6636939213254151586006006006007826066743741197278-81940697172828021542075167498588264571reponame:Repositório Institucional da UFGinstname:Universidade Federal de Goiás (UFG)instacron:UFGORIGINALDissertação - Achiles Silva Ferreira - 2018.pdfDissertação - Achiles Silva Ferreira - 2018.pdfapplication/pdf3183279http://repositorio.bc.ufg.br/tede/bitstreams/6f29713c-89b4-4379-afbb-522c1cb21dee/download59976d2d13952581ed03b3a3f2983a22MD55LICENSElicense.txtlicense.txttext/plain; charset=utf-82165http://repositorio.bc.ufg.br/tede/bitstreams/0c56f838-1c7c-406d-bf0b-ebae71df2ef7/downloadbd3efa91386c1718a7f26a329fdcb468MD51CC-LICENSElicense_urllicense_urltext/plain; charset=utf-849http://repositorio.bc.ufg.br/tede/bitstreams/6fd4e1d1-b6ac-46dd-ac6a-f93d748bbf53/download4afdbb8c545fd630ea7db775da747b2fMD52license_textlicense_texttext/html; charset=utf-80http://repositorio.bc.ufg.br/tede/bitstreams/bf20fd23-5e1b-4afe-9106-65f57e918705/downloadd41d8cd98f00b204e9800998ecf8427eMD53license_rdflicense_rdfapplication/rdf+xml; charset=utf-80http://repositorio.bc.ufg.br/tede/bitstreams/a7ce51b9-a709-40d5-8fab-4ae30a1f7b64/downloadd41d8cd98f00b204e9800998ecf8427eMD54tede/86792018-07-11 07:40:15.6http://creativecommons.org/licenses/by-nc-nd/4.0/Acesso Abertoopen.accessoai:repositorio.bc.ufg.br:tede/8679http://repositorio.bc.ufg.br/tedeRepositório InstitucionalPUBhttps://repositorio.bc.ufg.br/tedeserver/oai/requestgrt.bc@ufg.bropendoar:oai:repositorio.bc.ufg.br:tede/12342018-07-11T10:40:15Repositório Institucional da UFG - Universidade Federal de Goiás (UFG)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 |
| dc.title.eng.fl_str_mv |
Síntese de compostos heteroazóicos substituídos no solvente alternativo PEG 400 |
| dc.title.alternative.eng.fl_str_mv |
Synthesis of heteroazo compounds in alternative solvent PEG 400 |
| title |
Síntese de compostos heteroazóicos substituídos no solvente alternativo PEG 400 |
| spellingShingle |
Síntese de compostos heteroazóicos substituídos no solvente alternativo PEG 400 Ferreira, Achiles Silva Síntese Heterocíclicos Synthesis Heterocyclics QUIMICA::QUIMICA ORGANICA |
| title_short |
Síntese de compostos heteroazóicos substituídos no solvente alternativo PEG 400 |
| title_full |
Síntese de compostos heteroazóicos substituídos no solvente alternativo PEG 400 |
| title_fullStr |
Síntese de compostos heteroazóicos substituídos no solvente alternativo PEG 400 |
| title_full_unstemmed |
Síntese de compostos heteroazóicos substituídos no solvente alternativo PEG 400 |
| title_sort |
Síntese de compostos heteroazóicos substituídos no solvente alternativo PEG 400 |
| author |
Ferreira, Achiles Silva |
| author_facet |
Ferreira, Achiles Silva |
| author_role |
author |
| dc.contributor.advisor1.fl_str_mv |
Barros, Olga Soares do Rêgo |
| dc.contributor.advisor1Lattes.fl_str_mv |
http://lattes.cnpq.br/8311808341863723 |
| dc.contributor.advisor-co1.fl_str_mv |
Chagas, Rafael Pavão das |
| dc.contributor.advisor-co1Lattes.fl_str_mv |
http://lattes.cnpq.br/9712618482518275 |
| dc.contributor.referee1.fl_str_mv |
Barros, Olga Soares do Rêgo |
| dc.contributor.referee1Lattes.fl_str_mv |
http://lattes.cnpq.br/8311808341863723 |
| dc.contributor.referee2.fl_str_mv |
Chagas, Rafael Pavão das |
| dc.contributor.referee3.fl_str_mv |
Milani, Jorge Luiz Sônego |
| dc.contributor.referee4.fl_str_mv |
Costa, Maisa Borges |
| dc.contributor.authorLattes.fl_str_mv |
http://lattes.cnpq.br/7794429925120494 |
| dc.contributor.author.fl_str_mv |
Ferreira, Achiles Silva |
| contributor_str_mv |
Barros, Olga Soares do Rêgo Chagas, Rafael Pavão das Barros, Olga Soares do Rêgo Chagas, Rafael Pavão das Milani, Jorge Luiz Sônego Costa, Maisa Borges |
| dc.subject.por.fl_str_mv |
Síntese Heterocíclicos |
| topic |
Síntese Heterocíclicos Synthesis Heterocyclics QUIMICA::QUIMICA ORGANICA |
| dc.subject.eng.fl_str_mv |
Synthesis Heterocyclics |
| dc.subject.cnpq.fl_str_mv |
QUIMICA::QUIMICA ORGANICA |
| description |
The present work describes the development of a simple and efficient methodology for the synthesis of 2-aminoheteroazoic compounds using the solvent PEG 400 as an alternative to toxic and flammable organic solvents. Several media and reactional conditions were compared. A series of substituted 2-aminothiazoic compounds was obtained in good yields (60 to 96%) by a 3 hour reaction procedure using PEG 400 at room temperature and without the need for additives or catalysts. A selenium analogue and a 2-imino-1,3-thiazoline were also obtained by this method. The products were characterized by 1H and 13C NMR and infrared spectroscopies and mass spectrometry. The method covers some points of Green Chemistry, such as: safe synthesis, prevention in the formation of residues or derivatives, development of products that do not harm the environment, energy efficiency and accident prevention. |
| publishDate |
2018 |
| dc.date.accessioned.fl_str_mv |
2018-07-11T10:40:15Z |
| dc.date.issued.fl_str_mv |
2018-04-27 |
| 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.citation.fl_str_mv |
FERREIRA, A. S. Síntese de compostos heteroazóicos substituídos no solvente alternativo PEG 400. 2018. 76 f. Dissertação (Mestrado em Química) - Universidade Federal de Goiás, Goiânia, 2018. |
| dc.identifier.uri.fl_str_mv |
http://repositorio.bc.ufg.br/tede/handle/tede/8679 |
| dc.identifier.dark.fl_str_mv |
ark:/38995/0013000005t8t |
| identifier_str_mv |
FERREIRA, A. S. Síntese de compostos heteroazóicos substituídos no solvente alternativo PEG 400. 2018. 76 f. Dissertação (Mestrado em Química) - Universidade Federal de Goiás, Goiânia, 2018. ark:/38995/0013000005t8t |
| url |
http://repositorio.bc.ufg.br/tede/handle/tede/8679 |
| dc.language.iso.fl_str_mv |
por |
| language |
por |
| dc.relation.program.fl_str_mv |
663693921325415158 |
| dc.relation.confidence.fl_str_mv |
600 600 600 600 |
| dc.relation.department.fl_str_mv |
7826066743741197278 |
| dc.relation.cnpq.fl_str_mv |
-8194069717282802154 |
| dc.relation.sponsorship.fl_str_mv |
2075167498588264571 |
| dc.rights.driver.fl_str_mv |
http://creativecommons.org/licenses/by-nc-nd/4.0/ info:eu-repo/semantics/openAccess |
| rights_invalid_str_mv |
http://creativecommons.org/licenses/by-nc-nd/4.0/ |
| eu_rights_str_mv |
openAccess |
| dc.format.none.fl_str_mv |
application/pdf |
| dc.publisher.none.fl_str_mv |
Universidade Federal de Goiás |
| dc.publisher.program.fl_str_mv |
Programa de Pós-graduação em Química (IQ) |
| dc.publisher.initials.fl_str_mv |
UFG |
| dc.publisher.country.fl_str_mv |
Brasil |
| dc.publisher.department.fl_str_mv |
Instituto de Química - IQ (RG) |
| publisher.none.fl_str_mv |
Universidade Federal de Goiás |
| dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UFG instname:Universidade Federal de Goiás (UFG) instacron:UFG |
| instname_str |
Universidade Federal de Goiás (UFG) |
| instacron_str |
UFG |
| institution |
UFG |
| reponame_str |
Repositório Institucional da UFG |
| collection |
Repositório Institucional da UFG |
| bitstream.url.fl_str_mv |
http://repositorio.bc.ufg.br/tede/bitstreams/6f29713c-89b4-4379-afbb-522c1cb21dee/download http://repositorio.bc.ufg.br/tede/bitstreams/0c56f838-1c7c-406d-bf0b-ebae71df2ef7/download http://repositorio.bc.ufg.br/tede/bitstreams/6fd4e1d1-b6ac-46dd-ac6a-f93d748bbf53/download http://repositorio.bc.ufg.br/tede/bitstreams/bf20fd23-5e1b-4afe-9106-65f57e918705/download http://repositorio.bc.ufg.br/tede/bitstreams/a7ce51b9-a709-40d5-8fab-4ae30a1f7b64/download |
| bitstream.checksum.fl_str_mv |
59976d2d13952581ed03b3a3f2983a22 bd3efa91386c1718a7f26a329fdcb468 4afdbb8c545fd630ea7db775da747b2f d41d8cd98f00b204e9800998ecf8427e d41d8cd98f00b204e9800998ecf8427e |
| bitstream.checksumAlgorithm.fl_str_mv |
MD5 MD5 MD5 MD5 MD5 |
| repository.name.fl_str_mv |
Repositório Institucional da UFG - Universidade Federal de Goiás (UFG) |
| repository.mail.fl_str_mv |
grt.bc@ufg.br |
| _version_ |
1846536663236345856 |