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Synthesis of alkyl polyglycosides using SO(3)H-functionalized ionic liquids as catalysts
An effective process for synthesis of alkyl polyglycosides (APG) was developed using SO(3)H-functionalized ionic liquids (SFILs) as catalysts. Four SFILs, [PSmim][HSO(4)], [PSmim][pTSA], [PSPy][HSO(4)] and [PSPy][pTSA], were designed and synthesized for APG synthesis. The results indicated that [PSm...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8697811/ https://www.ncbi.nlm.nih.gov/pubmed/35423995 http://dx.doi.org/10.1039/d1ra00337b |
Sumario: | An effective process for synthesis of alkyl polyglycosides (APG) was developed using SO(3)H-functionalized ionic liquids (SFILs) as catalysts. Four SFILs, [PSmim][HSO(4)], [PSmim][pTSA], [PSPy][HSO(4)] and [PSPy][pTSA], were designed and synthesized for APG synthesis. The results indicated that [PSmim][HSO(4)] shows the best catalytic performance among these four SFILs, which has a great agreement with the order of their acidities. When the [PSmim][HSO(4)] was used as catalyst, the reaction time could be decreased from 24 h to 8 h, and molar ration of n-octanol to glucose could be decreased from 5 : 1 to 3 : 1 under the optimization reaction conditions. In addition, the [PSmim][HSO(4)] could be easily regenerated and recycled at least 5 times with slight decrease in catalytic activity. Moreover, the catalytic mechanism of [PSmim][HSO(4)] was further investigated by molecular simulation. The high catalytic activity of [PSmim][HSO(4)] is attributed to hydrogen bonds between [PSmim][HSO(4)] and glucose and n-octanol, which could accelerate the protonation of glucose and removal of hydrogen ions from the hydroxyl in n-octanol. |
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