Intensified, Kilogram-Scaled, and Environment-Friendly: Chemoenzymatic Synthesis of Bio-Based Acylated Hydroxystyrenes

Lignin-derived styrene derivatives are versatile building blocks for the manufacture of biobased polymers. As shown previously, phenol-protected hydroxystyrenes are accessible under industrially sound conditions (>100 g L<sup>-1</sup>, >95% yield) by subjecting biogenic phenolic acids to enzymatic decarboxylation and base-catalyzed acylation in nonaqueous media (wet cyclopentyl methyl ether, CPME). Herein, we demonstrate the production of 1 kg of 4-acetoxy-3-methoxy-styrene in a 10 L reactor and present practical adjustments to the up- and downstream processing that warrant a straightforward process and high isolated yields. Additionally, an environmental assessment is conducted, starting with a thorough <i>E</i> factor analysis to identify the sources that contribute most to the environmental burden (solvent and downstream processing). Also, the total CO<sub>2</sub> production of the process is studied, including contributions from energy use and the treatment of generated wastes. The energy impact is evaluated through thermodynamic analysis, and the environmental footprint contributions by wastes-organic and aqueous fractions-are assessed based on CO<sub>2</sub> emissions from solvent incineration and wastewater treatment, respectively. Overall, the holistic assessment of the process, its optimization, scale-up, product isolation, and environmental analysis indicate the feasibility of multistep chemoenzymatic reactions to deliver high-volume, low-value chemicals from biorefineries.

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Publication Details

Journal
ACS Sustainable Chemistry & Engineering
Published
2024-08-15
DOI
https://doi.org/10.1021/acssuschemeng.4c03648
Citations
11
Primary Topic
Enzyme Catalysis and Immobilization
Type
article
Field-Weighted Citation Impact
2.57

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article

Intensified, Kilogram-Scaled, and Environment-Friendly: Chemoenzymatic Synthesis of Bio-Based Acylated Hydroxystyrenes

Philipp Petermeier, María Domínguez, Emil Byström, Selin Kara
11 citations
ACS Sustainable Chemistry & Engineering
Enzyme Catalysis and Immobilization
2.57
article

Intensified, Kilogram-Scaled, and Environment-Friendly: Chemoenzymatic Synthesis of Bio-Based Acylated Hydroxystyrenes

Philipp Petermeier, María Domínguez, Emil Byström, Selin Kara
article en
11 citations

Abstract

Lignin-derived styrene derivatives are versatile building blocks for the manufacture of biobased polymers. As shown previously, phenol-protected hydroxystyrenes are accessible under industrially sound conditions (>100 g L<sup>-1</sup>, >95% yield) by subjecting biogenic phenolic acids to enzymatic decarboxylation and base-catalyzed acylation in nonaqueous media (wet cyclopentyl methyl ether, CPME). Herein, we demonstrate the production of 1 kg of 4-acetoxy-3-methoxy-styrene in a 10 L reactor and present practical adjustments to the up- and downstream processing that warrant a straightforward process and high isolated yields. Additionally, an environmental assessment is conducted, starting with a thorough <i>E</i> factor analysis to identify the sources that contribute most to the environmental burden (solvent and downstream processing). Also, the total CO<sub>2</sub> production of the process is studied, including contributions from energy use and the treatment of generated wastes. The energy impact is evaluated through thermodynamic analysis, and the environmental footprint contributions by wastes-organic and aqueous fractions-are assessed based on CO<sub>2</sub> emissions from solvent incineration and wastewater treatment, respectively. Overall, the holistic assessment of the process, its optimization, scale-up, product isolation, and environmental analysis indicate the feasibility of multistep chemoenzymatic reactions to deliver high-volume, low-value chemicals from biorefineries.

ACS Sustainable Chemistry & EngineeringVol. 12(34)
Leibniz University Hannover (DE), Aarhus University (DK)
European Commission, H2020 Marie Skłodowska-Curie Actions
Openalex Percentile: Top 10%
Enzyme Catalysis and Immobilization
2.57
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