Cycling of waste fusel alcohols from sugar cane industries using supercritical carbon dioxide
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Undergraduate course
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Royal Soc Chemistry
Royal Society of Chemistry (RSC)
Royal Society of Chemistry (RSC)
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Article
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Abstract
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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English
Citation
Rsc Advances. Cambridge: Royal Soc Chemistry, v. 5, n. 99, p. 81515-81522, 2015.






