A Reação de Diels - Alder de p-benzoquinonas sob efeito de microondas

Detalhes bibliográficos
Ano de defesa: 2008
Autor(a) principal: Donatoni, Maria Carolina
Orientador(a): Brocksom, Timothy John lattes
Banca de defesa: Não Informado pela instituição
Tipo de documento: Dissertação
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Federal de São Carlos
Programa de Pós-Graduação: Programa de Pós-Graduação em Química - PPGQ
Departamento: Não Informado pela instituição
País: BR
Palavras-chave em Português:
Área do conhecimento CNPq:
Link de acesso: https://repositorio.ufscar.br/handle/ufscar/6442
Resumo: In this work it was done a study of the microwave effect on Diels - Alder reaction of the p-benzoquinones thymoquinone (A1), 2,5-dimethyl-p-benzoquinone (A2) and 2,6-dimethyl-pbenzoquinone (A3) with the dienes cyclopentadiene (BB1), 2,3-dimethyl-1,3- butadiene (B2B ), isoprene (BB3) and trans-pyperilene (B4B ) (Figure Ι). These reactions were also held under conventional thermal conditions and catalysis with the Lewis acid SnCl4 in order to make a comparison of the results. It was also studied the Diels - Alder reaction in multicomponent version between thymoquinone (A1), trans-2-pentenal and acetamide under microwave effect (Figure ΙΙ). (FORMULA)Regarding the Diels - Alder reaction between p-benzoquinones (A1 - A3) and dienes (BB1 - B4B ) it was observed a reduction of the reaction time, obtaining higher yields and less formation of by - products, all in comparison with the results of the same reactions performed under thermal conventional condition and catalytic condition with SnCl4. This work also involved the study of the microwave effect on Diels - Alder reaction between cyclopentadiene (BB1) and mono-oximes dienophiles C1, C2 and C3 (Figure ΙΙΙ). These reactions had already been carried out in our laboratory, but under conventional thermal and catalytic conditions (Lewis acids). Under such conditions, the mono-oxime starting material was recovered, or a complex mixture of polymerization products was formed. (FORMULA)The reactions of compounds C1, C2 and C3 with cyclopentadiene (BB1) under microwave effect showed similar results with those that were obtained when these reactions were carried out under conventional thermal and catalytic conditions, thus leading to recovery of the mono-oxime starting material or a complex mixture of products which could not be identified.
id SCAR_dadfcfa1e026bcb95e6c71069b8f6f7b
oai_identifier_str oai:repositorio.ufscar.br:ufscar/6442
network_acronym_str SCAR
network_name_str Repositório Institucional da UFSCAR
repository_id_str
spelling Donatoni, Maria CarolinaBrocksom, Timothy Johnhttp://lattes.cnpq.br/7055452150201902http://lattes.cnpq.br/55047130694312532016-06-02T20:36:21Z2009-10-262016-06-02T20:36:21Z2008-08-08DONATONI, Maria Carolina. The diels-alder reaction of p-benzoquinones under microwave effect. 2008. 196 f. Dissertação (Mestrado em Ciências Exatas e da Terra) - Universidade Federal de São Carlos, São Carlos, 2008.https://repositorio.ufscar.br/handle/ufscar/6442In this work it was done a study of the microwave effect on Diels - Alder reaction of the p-benzoquinones thymoquinone (A1), 2,5-dimethyl-p-benzoquinone (A2) and 2,6-dimethyl-pbenzoquinone (A3) with the dienes cyclopentadiene (BB1), 2,3-dimethyl-1,3- butadiene (B2B ), isoprene (BB3) and trans-pyperilene (B4B ) (Figure Ι). These reactions were also held under conventional thermal conditions and catalysis with the Lewis acid SnCl4 in order to make a comparison of the results. It was also studied the Diels - Alder reaction in multicomponent version between thymoquinone (A1), trans-2-pentenal and acetamide under microwave effect (Figure ΙΙ). (FORMULA)Regarding the Diels - Alder reaction between p-benzoquinones (A1 - A3) and dienes (BB1 - B4B ) it was observed a reduction of the reaction time, obtaining higher yields and less formation of by - products, all in comparison with the results of the same reactions performed under thermal conventional condition and catalytic condition with SnCl4. This work also involved the study of the microwave effect on Diels - Alder reaction between cyclopentadiene (BB1) and mono-oximes dienophiles C1, C2 and C3 (Figure ΙΙΙ). These reactions had already been carried out in our laboratory, but under conventional thermal and catalytic conditions (Lewis acids). Under such conditions, the mono-oxime starting material was recovered, or a complex mixture of polymerization products was formed. (FORMULA)The reactions of compounds C1, C2 and C3 with cyclopentadiene (BB1) under microwave effect showed similar results with those that were obtained when these reactions were carried out under conventional thermal and catalytic conditions, thus leading to recovery of the mono-oxime starting material or a complex mixture of products which could not be identified.Neste trabalho foi feito um estudo do efeito das microondas sobre a reação de Diels - Alder das p-benzoquinonas timoquinona (A1), 2,5-dimetil-p-benzoquinona (A2) e 2,6-dimetil-p-benzoquinona (A3) com os dienos ciclopentadieno (B1), 2,3-dimetil-1,3-butadieno (B2), isopreno (B3), transpiperileno (B4) (Figura Ι). Estas reações foram realizadas também sob condições térmicas convencionais e de catálise com o ácido de Lewis, SnCl4, com intuito de se fazer a comparação dos resultados. (FORMULA) Foi estudada também a reação de Diels - Alder em versão multicomponente da timoquinona (A1) com o trans-2-pentenal e acetamida (Figura ΙΙ) sob efeito de microondas. (FORMULA) Em relação à reação de Diels - Alder das p-benzoquinonas (A1 - A3) com os dienos (BB1 - B4) foram observados uma redução dos tempos de reação, obtenção de maiores rendimentos e, portanto menor formação de subprodutos quando comparados com os resultados obtidos para as mesmas reações realizadas sob condições térmicas convencionais e sob condições de catálise com SnCl4. Este trabalho envolveu também o estudo do efeito de microondas sob a reação de Diels - Alder entre o ciclopentadieno (B1B ) e os dienófilos mono-oximas C1, C2 e C3 (Figura ΙΙΙ). Estas reações já haviam sido realizadas em nosso laboratório, porém sob condições térmicas convencionais ou de catálise com ácidos de Lewis. Sob tais condições obteve-se ou a recuperação do dienófilo de partida ou a uma mistura complexa de produtos de polimerização. (FORMULA) As reações dos compostos C1, C2, e C3 com ciclopentadieno (BB1) sob efeito de microondas mostraram resultados semelhantes a aqueles obtidos para as mesmas reações realizadas sob condições térmicas convencionais e de catálise com ácidos de Lewis, levando assim a recuperação do material de partida ou a uma mistura complexa de produtos, os quais não puderam ser identificados.Financiadora de Estudos e Projetosapplication/pdfporUniversidade Federal de São CarlosPrograma de Pós-Graduação em Química - PPGQUFSCarBRDiels-AlderMicroondasPara-BenzoquinonasCIENCIAS EXATAS E DA TERRA::QUIMICAA Reação de Diels - Alder de p-benzoquinonas sob efeito de microondasThe diels-alder reaction of p-benzoquinones under microwave effectinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFSCARinstname:Universidade Federal de São Carlos (UFSCAR)instacron:UFSCARORIGINAL2041.pdfapplication/pdf7286853https://{{ getenv "DSPACE_HOST" "repositorio.ufscar.br" }}/bitstream/ufscar/6442/1/2041.pdf5d9880838eb2486c513e5c444b5de019MD51THUMBNAIL2041.pdf.jpg2041.pdf.jpgIM Thumbnailimage/jpeg8974https://{{ getenv "DSPACE_HOST" "repositorio.ufscar.br" }}/bitstream/ufscar/6442/2/2041.pdf.jpgc3ff9c06e2cca6827b6ad41e1be02716MD52ufscar/64422019-09-11 02:57:59.772oai:repositorio.ufscar.br:ufscar/6442Repositório InstitucionalPUBhttps://repositorio.ufscar.br/oai/requestopendoar:43222023-05-25T12:51:17.549012Repositório Institucional da UFSCAR - Universidade Federal de São Carlos (UFSCAR)false
dc.title.por.fl_str_mv A Reação de Diels - Alder de p-benzoquinonas sob efeito de microondas
dc.title.alternative.eng.fl_str_mv The diels-alder reaction of p-benzoquinones under microwave effect
title A Reação de Diels - Alder de p-benzoquinonas sob efeito de microondas
spellingShingle A Reação de Diels - Alder de p-benzoquinonas sob efeito de microondas
Donatoni, Maria Carolina
Diels-Alder
Microondas
Para-Benzoquinonas
CIENCIAS EXATAS E DA TERRA::QUIMICA
title_short A Reação de Diels - Alder de p-benzoquinonas sob efeito de microondas
title_full A Reação de Diels - Alder de p-benzoquinonas sob efeito de microondas
title_fullStr A Reação de Diels - Alder de p-benzoquinonas sob efeito de microondas
title_full_unstemmed A Reação de Diels - Alder de p-benzoquinonas sob efeito de microondas
title_sort A Reação de Diels - Alder de p-benzoquinonas sob efeito de microondas
author Donatoni, Maria Carolina
author_facet Donatoni, Maria Carolina
author_role author
dc.contributor.authorlattes.por.fl_str_mv http://lattes.cnpq.br/5504713069431253
dc.contributor.author.fl_str_mv Donatoni, Maria Carolina
dc.contributor.advisor1.fl_str_mv Brocksom, Timothy John
dc.contributor.advisor1Lattes.fl_str_mv http://lattes.cnpq.br/7055452150201902
contributor_str_mv Brocksom, Timothy John
dc.subject.por.fl_str_mv Diels-Alder
Microondas
Para-Benzoquinonas
topic Diels-Alder
Microondas
Para-Benzoquinonas
CIENCIAS EXATAS E DA TERRA::QUIMICA
dc.subject.cnpq.fl_str_mv CIENCIAS EXATAS E DA TERRA::QUIMICA
description In this work it was done a study of the microwave effect on Diels - Alder reaction of the p-benzoquinones thymoquinone (A1), 2,5-dimethyl-p-benzoquinone (A2) and 2,6-dimethyl-pbenzoquinone (A3) with the dienes cyclopentadiene (BB1), 2,3-dimethyl-1,3- butadiene (B2B ), isoprene (BB3) and trans-pyperilene (B4B ) (Figure Ι). These reactions were also held under conventional thermal conditions and catalysis with the Lewis acid SnCl4 in order to make a comparison of the results. It was also studied the Diels - Alder reaction in multicomponent version between thymoquinone (A1), trans-2-pentenal and acetamide under microwave effect (Figure ΙΙ). (FORMULA)Regarding the Diels - Alder reaction between p-benzoquinones (A1 - A3) and dienes (BB1 - B4B ) it was observed a reduction of the reaction time, obtaining higher yields and less formation of by - products, all in comparison with the results of the same reactions performed under thermal conventional condition and catalytic condition with SnCl4. This work also involved the study of the microwave effect on Diels - Alder reaction between cyclopentadiene (BB1) and mono-oximes dienophiles C1, C2 and C3 (Figure ΙΙΙ). These reactions had already been carried out in our laboratory, but under conventional thermal and catalytic conditions (Lewis acids). Under such conditions, the mono-oxime starting material was recovered, or a complex mixture of polymerization products was formed. (FORMULA)The reactions of compounds C1, C2 and C3 with cyclopentadiene (BB1) under microwave effect showed similar results with those that were obtained when these reactions were carried out under conventional thermal and catalytic conditions, thus leading to recovery of the mono-oxime starting material or a complex mixture of products which could not be identified.
publishDate 2008
dc.date.issued.fl_str_mv 2008-08-08
dc.date.available.fl_str_mv 2009-10-26
2016-06-02T20:36:21Z
dc.date.accessioned.fl_str_mv 2016-06-02T20:36:21Z
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 DONATONI, Maria Carolina. The diels-alder reaction of p-benzoquinones under microwave effect. 2008. 196 f. Dissertação (Mestrado em Ciências Exatas e da Terra) - Universidade Federal de São Carlos, São Carlos, 2008.
dc.identifier.uri.fl_str_mv https://repositorio.ufscar.br/handle/ufscar/6442
identifier_str_mv DONATONI, Maria Carolina. The diels-alder reaction of p-benzoquinones under microwave effect. 2008. 196 f. Dissertação (Mestrado em Ciências Exatas e da Terra) - Universidade Federal de São Carlos, São Carlos, 2008.
url https://repositorio.ufscar.br/handle/ufscar/6442
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
dc.publisher.none.fl_str_mv Universidade Federal de São Carlos
dc.publisher.program.fl_str_mv Programa de Pós-Graduação em Química - PPGQ
dc.publisher.initials.fl_str_mv UFSCar
dc.publisher.country.fl_str_mv BR
publisher.none.fl_str_mv Universidade Federal de São Carlos
dc.source.none.fl_str_mv reponame:Repositório Institucional da UFSCAR
instname:Universidade Federal de São Carlos (UFSCAR)
instacron:UFSCAR
instname_str Universidade Federal de São Carlos (UFSCAR)
instacron_str UFSCAR
institution UFSCAR
reponame_str Repositório Institucional da UFSCAR
collection Repositório Institucional da UFSCAR
bitstream.url.fl_str_mv https://{{ getenv "DSPACE_HOST" "repositorio.ufscar.br" }}/bitstream/ufscar/6442/1/2041.pdf
https://{{ getenv "DSPACE_HOST" "repositorio.ufscar.br" }}/bitstream/ufscar/6442/2/2041.pdf.jpg
bitstream.checksum.fl_str_mv 5d9880838eb2486c513e5c444b5de019
c3ff9c06e2cca6827b6ad41e1be02716
bitstream.checksumAlgorithm.fl_str_mv MD5
MD5
repository.name.fl_str_mv Repositório Institucional da UFSCAR - Universidade Federal de São Carlos (UFSCAR)
repository.mail.fl_str_mv
_version_ 1767351098820001792