Cycling of waste fusel alcohols from sugar cane industries using supercritical carbon dioxide
Autor(a) principal: | |
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Data de Publicação: | 2015 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1039/c5ra16346c http://hdl.handle.net/11449/160886 |
Resumo: | The present study describes the clean synthesis of non-phosgene organic carbonates (NPOCs) from a selective multicomponent reaction with two important by-products from sugar and alcohol industries, namely, fusel alcohols and carbon dioxide, in the presence of 1,8-diazabicycloundecene (DBU), 1,5-diazabicyclo[4.3.0]-non-5-ene (DBN) or 1,3,4,6,7,8-hexahydro-2H-pyrimido[1,2-a]-pyrimidine (TBD) and an alkylating agent. The bases were used for the nucleophilic activation of the alcohols. The synthesis of carbonates was carried out without solvent and confirmed by GC-MS with EI ionization mode, H-1- and C-13-NMR and FT-IR analysis. The carbonates were obtained in excellent yields. Crude fusel alcohol can be converted to alkylcarbonates. The proposed methodology can also be employed to convert other hydroxylated compounds into carbonates. |
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Repositório Institucional da UNESP |
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spelling |
Cycling of waste fusel alcohols from sugar cane industries using supercritical carbon dioxideThe present study describes the clean synthesis of non-phosgene organic carbonates (NPOCs) from a selective multicomponent reaction with two important by-products from sugar and alcohol industries, namely, fusel alcohols and carbon dioxide, in the presence of 1,8-diazabicycloundecene (DBU), 1,5-diazabicyclo[4.3.0]-non-5-ene (DBN) or 1,3,4,6,7,8-hexahydro-2H-pyrimido[1,2-a]-pyrimidine (TBD) and an alkylating agent. The bases were used for the nucleophilic activation of the alcohols. The synthesis of carbonates was carried out without solvent and confirmed by GC-MS with EI ionization mode, H-1- and C-13-NMR and FT-IR analysis. The carbonates were obtained in excellent yields. Crude fusel alcohol can be converted to alkylcarbonates. The proposed methodology can also be employed to convert other hydroxylated compounds into carbonates.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Programa de Pos-graduacao em Ciencia e Tecnologia de Materiais (POSMAT)Univ Estadual Paulista, Fac Ciencias & Tecnol, Dept Fis Quim & Biol, Lab Quim Organ Fina CP 467, BR-19060900 Presidente Prudente, SP, BrazilUniv Estadual Paulista, Fac Ciencias & Tecnol, Dept Fis Quim & Biol, Lab Quim Organ Fina CP 467, BR-19060900 Presidente Prudente, SP, BrazilFAPESP: 2013/216680FAPESP: 2013/24487-6FAPESP: 2012/13901-3FAPESP: 2011/23438-6FAPESP: 2012/24330-7FAPESP: 2012/24661-3FAPESP: 2014/00289-3Royal Soc ChemistryUniversidade Estadual Paulista (Unesp)Pereira, F. S. [UNESP]Pereira, L. J. [UNESP]Credito, D. F. A. [UNESP]Girao, L. H. V. [UNESP]Idehara, A. H. S. [UNESP]Gonzalez, E. R. P. [UNESP]2018-11-26T16:17:08Z2018-11-26T16:17:08Z2015-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article81515-81522http://dx.doi.org/10.1039/c5ra16346cRsc Advances. Cambridge: Royal Soc Chemistry, v. 5, n. 99, p. 81515-81522, 2015.2046-2069http://hdl.handle.net/11449/16088610.1039/c5ra16346cWOS:000362436800076Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengRsc Advances0,863info:eu-repo/semantics/openAccess2021-10-23T15:48:17Zoai:repositorio.unesp.br:11449/160886Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462021-10-23T15:48:17Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Cycling of waste fusel alcohols from sugar cane industries using supercritical carbon dioxide |
title |
Cycling of waste fusel alcohols from sugar cane industries using supercritical carbon dioxide |
spellingShingle |
Cycling of waste fusel alcohols from sugar cane industries using supercritical carbon dioxide Pereira, F. S. [UNESP] |
title_short |
Cycling of waste fusel alcohols from sugar cane industries using supercritical carbon dioxide |
title_full |
Cycling of waste fusel alcohols from sugar cane industries using supercritical carbon dioxide |
title_fullStr |
Cycling of waste fusel alcohols from sugar cane industries using supercritical carbon dioxide |
title_full_unstemmed |
Cycling of waste fusel alcohols from sugar cane industries using supercritical carbon dioxide |
title_sort |
Cycling of waste fusel alcohols from sugar cane industries using supercritical carbon dioxide |
author |
Pereira, F. S. [UNESP] |
author_facet |
Pereira, F. S. [UNESP] Pereira, L. J. [UNESP] Credito, D. F. A. [UNESP] Girao, L. H. V. [UNESP] Idehara, A. H. S. [UNESP] Gonzalez, E. R. P. [UNESP] |
author_role |
author |
author2 |
Pereira, L. J. [UNESP] Credito, D. F. A. [UNESP] Girao, L. H. V. [UNESP] Idehara, A. H. S. [UNESP] Gonzalez, E. R. P. [UNESP] |
author2_role |
author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (Unesp) |
dc.contributor.author.fl_str_mv |
Pereira, F. S. [UNESP] Pereira, L. J. [UNESP] Credito, D. F. A. [UNESP] Girao, L. H. V. [UNESP] Idehara, A. H. S. [UNESP] Gonzalez, E. R. P. [UNESP] |
description |
The present study describes the clean synthesis of non-phosgene organic carbonates (NPOCs) from a selective multicomponent reaction with two important by-products from sugar and alcohol industries, namely, fusel alcohols and carbon dioxide, in the presence of 1,8-diazabicycloundecene (DBU), 1,5-diazabicyclo[4.3.0]-non-5-ene (DBN) or 1,3,4,6,7,8-hexahydro-2H-pyrimido[1,2-a]-pyrimidine (TBD) and an alkylating agent. The bases were used for the nucleophilic activation of the alcohols. The synthesis of carbonates was carried out without solvent and confirmed by GC-MS with EI ionization mode, H-1- and C-13-NMR and FT-IR analysis. The carbonates were obtained in excellent yields. Crude fusel alcohol can be converted to alkylcarbonates. The proposed methodology can also be employed to convert other hydroxylated compounds into carbonates. |
publishDate |
2015 |
dc.date.none.fl_str_mv |
2015-01-01 2018-11-26T16:17:08Z 2018-11-26T16:17:08Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1039/c5ra16346c Rsc Advances. Cambridge: Royal Soc Chemistry, v. 5, n. 99, p. 81515-81522, 2015. 2046-2069 http://hdl.handle.net/11449/160886 10.1039/c5ra16346c WOS:000362436800076 |
url |
http://dx.doi.org/10.1039/c5ra16346c http://hdl.handle.net/11449/160886 |
identifier_str_mv |
Rsc Advances. Cambridge: Royal Soc Chemistry, v. 5, n. 99, p. 81515-81522, 2015. 2046-2069 10.1039/c5ra16346c WOS:000362436800076 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Rsc Advances 0,863 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
81515-81522 |
dc.publisher.none.fl_str_mv |
Royal Soc Chemistry |
publisher.none.fl_str_mv |
Royal Soc Chemistry |
dc.source.none.fl_str_mv |
Web of Science reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
|
_version_ |
1797789758215159808 |