University of Lincoln
Browse

Synthesis of Biobased Diethyl Terephthalate via Diels-Alder Addition of Ethylene to 2,5-Furandicarboxylic Acid Diethyl Ester: An Alternative Route to 100% Biobased Poly(ethylene terephthalate)

Version 2 2024-03-13, 10:04
Version 1 2023-12-20, 12:34
journal contribution
posted on 2024-03-13, 10:04 authored by J. K. Ogunjobi, T. J. Farmer, Con McElroyCon McElroy, S. W. Breeden, D. J. MacQuarrie, D. Thornthwaite, J. H. Clark
<p>Poly(ethylene terephthalate) (PET) is a ubiquitous thermoplastic currently produced from nonrenewable fossil resources; as such, sustainable biobased routes to the key terephthalate monomer are being widely pursued. Herein is demonstrated a greener solventless route to biobased diethyl terephthalate via a one-pot heterogeneous Lewis acid catalyzed Diels-Alder addition and dehydration of 2,5-furandicarboxylic acid diethyl ester with ethylene, giving yields of terephthalate up to 59% for the key Diels-Alder addition step. A metrics-based comparison against alternative published biobased routes (available from sugars, cellulose and hemicellulose) shows that the clean synthetic pathway developed herein gives a practical atom economy, overall yield and selectivity, making it a viable alternative to routes currently under development.</p>

History

School affiliated with

  • School of Chemistry (Research Outputs)

Publication Title

ACS Sustainable Chemistry & Engineering

Volume

7

Issue

9

Publisher

American Chemical Society

ISSN

2168-0485

Date Submitted

2023-06-06

Date Accepted

2019-04-16

Date of First Publication

2019-05-06

Date of Final Publication

2019-05-06

ePrints ID

54749

Usage metrics

    University of Lincoln (Research Outputs)

    Licence

    Exports

    RefWorks
    BibTeX
    Ref. manager
    Endnote
    DataCite
    NLM
    DC