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Published on: June 16, 2022
Bio-based building blocks from 5-hydroxymethylfurfural via 1-hydroxyhexane-2,5-dione as intermediate
Bartosz Wozniak1, Sergey Tin1, Johannes G de Vries1
1Leibniz-Institut für Katalyse e.V. , Universität Rostock , Albert-Einstein-Str.29a , 18059 Rostock , Germany .
Biomass-derived 5-hydroxymethylfurfural (HMF) can be converted to 1-hydroxyhexane-2,5-dione (HHD) using catalytic hydrogenation. This review covers HHD synthesis and its applications as a versatile chemical building block.
Area of Science:
- Chemical Engineering
- Organic Chemistry
- Sustainable Chemistry
Background:
- Fossil resource depletion necessitates alternative fuel and chemical sources.
- Biomass offers a renewable feedstock for valuable platform chemicals.
- 5-hydroxymethylfurfural (HMF) is a key biomass-derived platform chemical with broad conversion potential.
Purpose of the Study:
- To review the synthesis of 1-hydroxyhexane-2,5-dione (HHD) from HMF.
- To explore the mechanistic aspects of HHD formation.
- To highlight recent advancements in HHD applications as a chemical precursor.
Main Methods:
- Catalytic hydrogenation and hydrolytic ring opening of HMF in aqueous phase.
- Utilizing both heterogeneous and homogeneous catalysts for HMF conversion.
- Reviewing literature on HHD synthesis pathways and reaction mechanisms.
Main Results:
- HMF can be efficiently converted to HHD through hydrogenation/hydrolytic ring opening.
- Various catalytic systems have been developed for this transformation.
- HHD serves as a versatile intermediate for synthesizing pyrroles, cyclopentanones, and triols.
Conclusions:
- The conversion of HMF to HHD is a promising route for sustainable chemical production.
- HHD is a valuable building block for a diverse range of chemical products.
- Further research into HHD synthesis and applications can advance green chemistry initiatives.
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