Merging Lignin and Glycerol Carbonate Valorization Toward the Green Synthesis of <i>β</i> ‐Adrenergic Blocker Esmolol

Producing nitrogen-containing chemicals through the direct combination of by-products readily available from agricultural waste, including renewable aromatic building blocks from lignin, is a highly attractive approach for sustainable biorefining processes. Here, we describe a novel synthetic/catalytic route toward the production of the highly valuable β-adrenergic blocker esmolol. Our strategy consists of: 1) Reductive Catalytic Fractionation (RCF) of sugarcane lignocellulose mediated by copper porous metal oxides (Cu<sub>20</sub>PMO) in MeOH, leading to the in situ formation of methyl 3-(4-hydroxyphenyl) propionate (1H) with good selectivity (>70%), followed by 2) the selective catalytic amination of glycerol carbonate (GlyC) with isopropyl amine via the borrowing hydrogen strategy, and 3) the subsequent utilization of the obtained amine intermediate as a phenol alkylating agent in combination with 1H to afford the desired β-adrenergic blocker esmolol (1Ha).

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Journal
ChemSusChem
Published
2025-12-14
DOI
https://doi.org/10.1002/cssc.202501540
Primary Topic
Carbon dioxide utilization in catalysis
Type
article
Field-Weighted Citation Impact
0.00

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article

Merging Lignin and Glycerol Carbonate Valorization Toward the Green Synthesis of β ‐Adrenergic Blocker Esmolol

Katalin Barta, Antonio A. Castillo‐Garcia
ChemSusChem
Carbon dioxide utilization in catalysis
article

Merging Lignin and Glycerol Carbonate Valorization Toward the Green Synthesis of β ‐Adrenergic Blocker Esmolol

Katalin Barta, Antonio A. Castillo‐Garcia
article en

Abstract

Producing nitrogen-containing chemicals through the direct combination of by-products readily available from agricultural waste, including renewable aromatic building blocks from lignin, is a highly attractive approach for sustainable biorefining processes. Here, we describe a novel synthetic/catalytic route toward the production of the highly valuable β-adrenergic blocker esmolol. Our strategy consists of: 1) Reductive Catalytic Fractionation (RCF) of sugarcane lignocellulose mediated by copper porous metal oxides (Cu<sub>20</sub>PMO) in MeOH, leading to the in situ formation of methyl 3-(4-hydroxyphenyl) propionate (1H) with good selectivity (>70%), followed by 2) the selective catalytic amination of glycerol carbonate (GlyC) with isopropyl amine via the borrowing hydrogen strategy, and 3) the subsequent utilization of the obtained amine intermediate as a phenol alkylating agent in combination with 1H to afford the desired β-adrenergic blocker esmolol (1Ha).

ChemSusChemVol. 19(1)
Graz University of Technology (AT)
Austrian Science Fund
Openalex Percentile: Top 68%
Carbon dioxide utilization in catalysis
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Merging Lignin and Glycerol Carbonate Valorization Toward the Green Synthesis of <i>β</i> ‐Adrenergic Blocker Esmolol — Katalin Barta, Antonio A. Castillo‐Garcia · ChemSusChem (2025) | TGRS Research Map | TGRS