5-Hydroxymethylfurfural (HMF) synthesis in a deep eutectic solvent-based biphasic system: closing the loop of solvent reuse, product isolation and green metrics†

Nico Thanheuser, Leonie Schlichter, Walter Leitner, Jesús Esteban and Andreas J. Vorholt
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Abstract

The scale up and recycling of all process streams in the H4SiW12O40 catalyzed dehydration of D-fructose (Fru) to 5-hydroxymethylfurfural (HMF) were investigated. For this, a biphasic system based on a self-consuming deep eutectic solvent (DES) consisting of choline chloride (ChCl) and Fru in a molar ratio of 5 : 1 as the reaction phase with in situ extraction of HMF employing acetonitrile was employed. In addition to ChCl : Fru being a cost-effective DES of renewable origin, it provides a way to suppress side reactions to levulinic and formic acid, particularly. The scale-up of the reaction system to a total volume of 180 mL resulted in a reaction time of 12.5 minutes to achieve quantitative conversion reaching high yields of 76% and selectivities as high as 83% whilst operating temperature was only at 80 °C, while proceeding twice as fast compared to the smaller scale reaction of previous work. The system shows easy separation of the upper extraction phase from the reaction phase due to the solidification of ChCl and the catalyst H4SiW12O40 upon cooling to room temperature showing partition coefficients of about 4 to 5. HMF could be isolated from the extraction phase, recovering HMF crystals of >99% purity. The system has the potential for numerous recycling runs up to a water content of 7.5 wt%, beyond which the DES phase undergoes a loss of activity due to the system transitioning to an aqueous solution. The extraction phase shows full recyclability and can be reused after simple distillation to separate HMF, showing promise for further implementation. Finally, considering the mass balance of the system, the basic green metrics of the system are calculated to show its potential compared to other similar concepts in the literature.

Abstract Image

5-羟甲基糠醛(HMF)在深共晶溶剂基双相体系中的合成:溶剂再利用、产物分离和绿色指标的闭环
研究了H4SiW12O40催化d -果糖(Fru)脱水制5-羟甲基糠醛(HMF)各工艺流程的规模放大和循环利用情况。为此,采用由氯化胆碱(ChCl)和氟(Fru)组成的自消耗深度共晶溶剂(DES),摩尔比为5:1的双相体系作为反应相,用乙腈原位提取HMF。除了ChCl: Fru是一种具有成本效益的可再生DES来源外,它还提供了一种抑制乙酰丙酸和甲酸的副反应的方法,特别是。将反应系统的体积扩大到180 mL,反应时间为12.5分钟,在操作温度仅为80℃的情况下实现了76%的高产率和83%的选择性的定量转化,同时进行速度是之前工作的小规模反应的两倍。由于ChCl和催化剂H4SiW12O40在冷却至室温后凝固,该体系易于从反应相中分离出上部萃取相,其分割系数约为4 ~ 5。从萃取相中可以分离出HMF,回收纯度为99%的HMF晶体。该系统具有多次循环运行的潜力,含水量可达7.5 wt%,超过此含量,由于系统转变为水溶液,DES相将失去活性。萃取阶段表现出完全可回收性,可以在简单蒸馏后重复使用以分离HMF,显示出进一步实施的前景。最后,考虑到系统的质量平衡,计算了系统的基本绿色指标,以显示其与文献中其他类似概念相比的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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