Lignin-based bisguaiacol diisocyanate: a green route for the synthesis of biobased polyurethanes

The synthesis of a new biobased aromatic diisocyanate derived from lignocellulosic raw material, namely guaiacol and vanillyl alcohol, through phosgene-free route offers the prospect of greener approaches for isocyanate production and the polyurethane industry. Indeed, bisguaiacol F diisocyanate (BG...

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Veröffentlicht in:Green chemistry : an international journal and green chemistry resource : GC 2023-06, Vol.25 (12), p.4833-4839
Hauptverfasser: Lemouzy, Sébastien, Delavarde, Aliénor, Lamaty, Frédéric, Bantreil, Xavier, Pinaud, Julien, Caillol, Sylvain
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Sprache:eng
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Zusammenfassung:The synthesis of a new biobased aromatic diisocyanate derived from lignocellulosic raw material, namely guaiacol and vanillyl alcohol, through phosgene-free route offers the prospect of greener approaches for isocyanate production and the polyurethane industry. Indeed, bisguaiacol F diisocyanate (BGI) was obtained via a three-step process from readily available bisguaiacol F (BGF), involving conversion of aromatic amine into aromatic isocyanate. The unusual transition-metal-free conversion of BGF to bisguaiacol F diamine (BGA) was performed by a two-step approach: (a) the Williamson-type alkylation of BGF and then (b) the base-promoted Smiles rearrangement of bis O -alkylated BGF. In order to improve the sustainability of this process, the first step was realized under solvent-free mechanochemical conditions, and the second step was performed using two different activating methods: thermal and microwave. The thermal process provided an isolated BGA yield of ca. 70%. Microwave activation proved to be an interesting alternative, although a lower yield (32%) of the desired BGA was achieved. Finally, the diisocyanate synthesis was performed via a phosgene-free/room temperature protocol using di- tert -butyl dicarbonate in the presence of a catalytic amount of 4-dimethylaminopyridine (DMAP). Two polyurethane thermosets were designed and synthesized using the aromatic diisocyanates, biobased BGI and petrochemical-based methylene diphenyl diisocyanate (MDI), by a solvent-free two-step polymerization. Their thermo-chemical properties as well as their reactivities for polymer synthesis were evaluated. These preliminary results suggest that BGI could be potentially used as a nearly fully biobased surrogate for MDI. The synthesis of aromatic diisocyanate derived from lignocellulosic raw materials, namely guaiacol and vanillyl alcohol, through phosgene-free route offers the prospect of greener approaches for isocyanate production and the polyurethane industry.
ISSN:1463-9262
1463-9270
DOI:10.1039/d3gc00704a