Studies on the Reactions of Lactone Intermediates Derived from Levulinic Acid: Telescoped Routes to Higher Levulinate Ester Biofuels
Year: 2025
Type: article
Abstract: The development of efficient strategies for the synthesis of levulinate esters is of significant current interest due to their potential as biofuels and fuel additives. Herein, we report a novel strategy to access levulinate esters derived from higher alcohols directly from levulinic acid through the in situ generation of lactone intermediates employing commercial heterogeneous catalysts, such as Amberlyst-15. This strategy employs a telescoped approach in which the lactonization/ring-opening reactions are combined into an operationally simple one-pot procedure. This strategy is advantageous as it employs a readily available and inexpensive catalyst and proceeds in short reaction times to produce excellent yields of higher levulinate esters with high selectivity. Furthermore, the Amberlyst-15 catalyst is fully recyclable and can be reused without loss of activity or selectivity.
Source: ACS Omega
Institutions: University of South Wales, Cardiff University
Language: English
Subfield: Biomedical Engineering
Field: Engineering
Domain: Physical Sciences
Open Access status: gold
Estimated APC paid: $1,935
Funder: Leverhulme Trust
Award: G6846567295
OpenAlex ID: W4409134785
