Proof of concept for continuous enantioselective liquid–liquid extraction in capillary microreactors using 1-octanol as a sustainable solvent
The use of capillary microreactors for enantioselective liquid–liquid extraction (ELLE) was successfully demonstrated using a model system consisting of a buffered aqueous amino acid derivative (3,5-dinitrobenzoyl-( R , S )-leucine) solution (phosphate buffer, pH 6.58) and a chiral cinchona alkaloid...
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Veröffentlicht in: | Green chemistry : an international journal and green chemistry resource : GC 2017, Vol.19 (18), p.4334-4343 |
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Hauptverfasser: | , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The use of capillary microreactors for enantioselective liquid–liquid extraction (ELLE) was successfully demonstrated using a model system consisting of a buffered aqueous amino acid derivative (3,5-dinitrobenzoyl-(
R
,
S
)-leucine) solution (phosphate buffer, pH 6.58) and a chiral cinchona alkaloid (CA) host in an organic solvent. It was shown that 1-octanol is a suitable replacement for the commonly used chlorinated solvents like 1,2-dichloroethane. Experiments were conducted in a capillary microreactor set-up (0.8 mm internal diameter) operated in the slug flow regime at 294 K (residence times between 12 and 900 s, 1 : 1 flow ratio of the aqueous to organic phases, 1 mM of host and 1 mM of amino acid derivative). The enantiomeric excess (ee) was shown to be a function of the solvent and residence time and varied between 37% and 49% in 1,2-DCE and 28 and 46% in 1-octanol in the organic phase. The ee values in the organic phase at shorter residence times were higher than the independently determined equilibrium ee values (41% in 1,2-DCE and 31% in 1-octanol at a host concentration of 1 mM). This is an unprecedented observation with large implications for ELLE, as it implies that operation in the kinetic regime may lead to improved enantioseparation performance. |
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ISSN: | 1463-9262 1463-9270 |
DOI: | 10.1039/C7GC01700F |