Renewable Thiophene Synthesis from Biomass Derived Methyl Levulinate and Elemental Sulfur
Heterocyclic compounds are pivotal building blocks in petrochemical and renewable fine chemical synthesis. The production of bio-based heterocyclic compounds is limited to furans and pyrroles, while thiophenes are rarely prepared from bio-based feedstock in a real renewable method. Current research on the "pseudo-renewable" thiophene synthesis strongly relies on unwieldy Lawesson's Reagent, which makes the process unsustainable. The present work describes for the first time that, two thiophene diesters were synthesized from biomass-derived methyl levulinate and elemental sulfur, a cheap, surplus by-product of the fossil industry that is causing potential pollution. The condensation and sulfurization steps in this process all involved multiple reaction pathways, leading to a much more intricate mechanism than previous research in its type. The footprint of sulfur in this system was tracked throughout the process, and the chemistry of this multi-step reaction provided a new orientation for the real sustainable thiophene synthesis based on elemental sulfur.
Authors
- Xianhai Zeng (ORCID: https://orcid.org/0000-0002-5441-3164)
- Zheng Li (ORCID: https://orcid.org/0000-0003-4745-2090)
- Zhendong Yu (ORCID: https://orcid.org/0000-0001-5507-7679)
- Yining Zhang (ORCID: https://orcid.org/0000-0003-0128-1863)
- Qing Rui Yin (ORCID: https://orcid.org/0000-0001-9737-3265)
Institutions
- Xiamen University (CN)
- Collaborative Innovation Center of Chemistry for Energy Materials (CN)
Publication Details
- Journal
- ChemSusChem
- Published
- 2025-03-11
- DOI
- https://doi.org/10.1002/cssc.202500433
- Citations
- 1
- Primary Topic
- Organic Chemistry Cycloaddition Reactions
- Type
- article
- Field-Weighted Citation Impact
- 0.94