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–1, >95% yield) by subjecting biogenic phenolic acids to enzymatic decarb...

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Veröffentlicht in:ACS sustainable chemistry & engineering 2024-08, Vol.12 (34), p.12869-12878
Hauptverfasser: Petermeier, Philipp, Domínguez de María, Pablo, Byström, Emil, Kara, Selin
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container_end_page 12878
container_issue 34
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container_title ACS sustainable chemistry & engineering
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creator Petermeier, Philipp
Domínguez de María, Pablo
Byström, Emil
Kara, Selin
description 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–1, >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 E factor analysis to identify the sources that contribute most to the environmental burden (solvent and downstream processing). Also, the total CO2 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 CO2 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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Eng</addtitle><date>2024-08-26</date><risdate>2024</risdate><volume>12</volume><issue>34</issue><spage>12869</spage><epage>12878</epage><pages>12869-12878</pages><issn>2168-0485</issn><eissn>2168-0485</eissn><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 (&gt;100 g L–1, &gt;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. 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subjects acylation
biorefining
carbon dioxide
decarboxylation
ecological footprint
energy
environmental assessment
factor analysis
green chemistry
manufacturing
methyl ethers
solvents
styrene
thermodynamics
wastewater treatment
title Intensified, Kilogram-Scaled, and Environment-Friendly: Chemoenzymatic Synthesis of Bio-Based Acylated Hydroxystyrenes
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