Cycling of waste fusel alcohols from sugar cane industries using supercritical carbon dioxide

Detalhes bibliográficos
Autor(a) principal: Pereira, F. S. [UNESP]
Data de Publicação: 2015
Outros Autores: Pereira, L. J. [UNESP], Credito, D. F. A. [UNESP], Girao, L. H. V. [UNESP], Idehara, A. H. S. [UNESP], Gonzalez, E. R. P. [UNESP]
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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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
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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)
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