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Selection of deep eutectic solvents for supported liquid membrane extraction of chiral amines

(2023)

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Echezuria_82861800_2023.pdf
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Abstract
Chiral amines play an important role in the pharmaceutical domain. However, their synthesis methods continue to pose significant challenges, resulting in costly and non-environmentally friendly processes or unfavorable equilibria. This thesis introduces a technique that addresses these challenges by employing membrane extraction for the in-situ removal of target compounds, specifically focusing on 1-phenylethylamine (MBA) and 1-methyl-3-phenylpropylamine (MPPA) from the donor amine isopropylamine (IPA). The core of this thesis revolves around the exploration and characterization of deep eutectic solvents (DESs) that were pre-selected based on their selectivity towards the target amines over the donor amine, as determined through COSMO-RS simulations. The primary properties under scrutiny encompass selectivity, hydrogen bond acceptor and donor moments, viscosity, phase miscibility, and membrane stability. Out of forty-six mixtures evaluated, three exhibited the desired attributes crucial for the success of the supported liquid membrane (SLM) process, ensuring a lack of diffusion during experimentation. These three promising mixtures consist of trioctylphosphine oxide in combination with octanoic acid, menthol and thymol. Among these mixtures, the trioctylphosphine oxide-thymol combination exhibited the highest selectivity value towards the targeted amines and stability duringt the membrane extraction process.

Citations

Echezuria, C. (2023). Selection of deep eutectic solvents for supported liquid membrane extraction of chiral amines. https://dial-mem.test.bib.ucl.ac.be/handle/2078.2/34208