Aldred, Matthew P., Davies, Thomas E., Taylor, Stuart H. ![]() ![]() |
Preview |
PDF
- Published Version
Available under License Creative Commons Attribution Non-commercial No Derivatives. Download (1MB) | Preview |
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.
Item Type: | Article |
---|---|
Date Type: | Published Online |
Status: | In Press |
Schools: | Schools > Chemistry Research Institutes & Centres > Cardiff Catalysis Institute (CCI) |
Publisher: | American Chemical Society |
ISSN: | 2470-1343 |
Date of First Compliant Deposit: | 17 March 2025 |
Date of Acceptance: | 17 December 2024 |
Last Modified: | 07 Apr 2025 13:34 |
URI: | https://orca.cardiff.ac.uk/id/eprint/176905 |
Actions (repository staff only)
![]() |
Edit Item |