4.6 Article

Synthesis of alkyl polyglycosides using SO3H-functionalized ionic liquids as catalysts

Journal

RSC ADVANCES
Volume 11, Issue 24, Pages 14710-14716

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1ra00337b

Keywords

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Funding

  1. National Natural Science Foundation of China [22078323, 51574215, 21436010]

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The study found that [PSmim][HSO4] is the most effective catalyst among the four SFILs tested, significantly reducing reaction time and decreasing the ratio of n-octanol to glucose. Additionally, [PSmim][HSO4] can be easily regenerated and reused multiple times.
An effective process for synthesis of alkyl polyglycosides (APG) was developed using SO3H-functionalized ionic liquids (SFILs) as catalysts. Four SFILs, [PSmim][HSO4], [PSmim][pTSA], [PSPy][HSO4] and [PSPy][pTSA], were designed and synthesized for APG synthesis. The results indicated that [PSmim][HSO4] shows the best catalytic performance among these four SFILs, which has a great agreement with the order of their acidities. When the [PSmim][HSO4] 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][HSO4] could be easily regenerated and recycled at least 5 times with slight decrease in catalytic activity. Moreover, the catalytic mechanism of [PSmim][HSO4] was further investigated by molecular simulation. The high catalytic activity of [PSmim][HSO4] is attributed to hydrogen bonds between [PSmim][HSO4] 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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