scholarly journals One pot conversion of glucose to ethyl levulinate over a porous hydrothermal acid catalyst in green solvents

RSC Advances ◽  
2019 ◽  
Vol 9 (35) ◽  
pp. 20341-20344 ◽  
Author(s):  
Monika Bosilj ◽  
Johannes Schmidt ◽  
Anna Fischer ◽  
Robin J. White

One-pot conversion of glucose to ethyl levulinate over an acid-functionalised hydrothermal carbon gives high initial yields up to 37 mol% (comparable to H2SO4) with catalyst performance strongly influenced by green solvent choice.

2011 ◽  
Vol 14 (3) ◽  
pp. 79-86
Author(s):  
Nam Thanh Son Phan ◽  
Ha Vu Le

An easily accessible ionic liquid, 1-butyl-3-methylimidazolium hexafluorophosphate ([BMIM][PF6]) was synthesized, and characterized using 1H and 13C NMR, and MS. The ionic liquid was demonstrated to be an efficient green solvent for the synthesis of pravadoline, one of non-steroidal drugs. High yield was achieved without the presence of an anhydrous Lewis acid catalyst. The reaction was also successfully carried out using other imidazolium-based ionic liquids, including 1-hexyl-3-methylimidazolium hexafluorophosphate ([HMIM][PF6]), and 1-octyl-3- methylimidazolium hexafluorophosphate ([OMIM][PF6]). To our best knowledge, this is the first report in Viet Nam on the synthesis of a pharmaceutical chemical in ionic liquids as green solvents.


2020 ◽  
Vol 5 (8) ◽  
pp. 1405-1409 ◽  
Author(s):  
Surachai Karnjanakom ◽  
Asep Bayu ◽  
Panya Maneechakr ◽  
Chanatip Samart ◽  
Suwadee Kongparakul ◽  
...  

Ethyl levulinate was easily produced via one-pot conversion of sucrose under a reusable biphasic system over an active/stable acid catalyst.


2020 ◽  
Vol 60 (4) ◽  
pp. 499-507
Author(s):  
Maria Victoria Lopez-Prado ◽  
María J. Sabater ◽  
Avelino Corma

Tetrahedron ◽  
2006 ◽  
Vol 62 (17) ◽  
pp. 4059-4064 ◽  
Author(s):  
Rina Ghosh ◽  
Swarupananda Maiti ◽  
Arijit Chakraborty ◽  
Santu Chakraborty ◽  
Alok K. Mukherjee

2018 ◽  
Vol 14 ◽  
pp. 1655-1659 ◽  
Author(s):  
Ugo Azzena ◽  
Massimo Carraro ◽  
Gloria Modugno ◽  
Luisa Pisano ◽  
Luigi Urtis

The application of heterogeneous catalysis and green solvents to the set up of widely employed reactions is a challenge in contemporary organic chemistry. We applied such an approach to the synthesis and further conversion of tetrahydropyranyl ethers, an important class of compounds widely employed in multistep syntheses. Several alcohols and phenols were almost quantitatively converted into the corresponding tetrahydropyranyl ethers in cyclopentyl methyl ether or 2-methyltetrahydrofuran employing NH4HSO4 supported on SiO2 as a recyclable acidic catalyst. Easy work up of the reaction mixtures and the versatility of the solvents allowed further conversion of the reaction products under one-pot reaction conditions.


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