Isolation of two major sesquiterpenes from the leaf essential oil of Eugenia uniflora by preparative‐scale high‐speed countercurrent chromatography

The high‐speed countercurrent chromatography technique was employed to isolate two major compounds from the leaf essential oil of Eugenia uniflora L. (Myrtaceae). The volatile extract of Eugenia uniflora obtained by hydrodistillation was analyzed by gas chromatography coupled with flame ionization d...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Separation science plus 2018-12, Vol.1 (12), p.785-792
Hauptverfasser: Marques, André M., Aquino, Victor Hugo C., Correia, Virginia G., Siani, Antonio Carlos, Tappin, Marcelo Raul R., Kaplan, Maria Auxiliadora C., Figueiredo, Maria Raquel
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:The high‐speed countercurrent chromatography technique was employed to isolate two major compounds from the leaf essential oil of Eugenia uniflora L. (Myrtaceae). The volatile extract of Eugenia uniflora obtained by hydrodistillation was analyzed by gas chromatography coupled with flame ionization detection and gas chromatography coupled with mass spectrometry and shown to be almost exclusively constituted by sesquiterpenes, in which (+/‐)‐selina‐1,3,7(11)‐trien‐8‐one (A) and (+/‐)‐selina‐1,3,7(11)‐trien‐8‐one epoxide (B) were largely predominant. These two major compounds were separated by submitting the crude essential oil to countercurrent chromatography using hexane/acetonitrile 1:1 v/v as the solvent system, running in both the tail‐to‐head (mode I) and head‐to‐tail (mode II) modes. Upon running in mode I, a single application of the crude oil (800 mg) in the separation equipment coil afforded 78.2 mg of B (> 97.5% purity). Running in mode II produced 24.7 mg of A (92.5% purity) and 46.3 mg (93.1% purity) of B. The purity of each compound was determined by GC. For the first time, this technique was shown to be efficient to separate sesquiterpenes that are structurally very similar, affording high‐purity products in a short time with significant solvent savings.
ISSN:2573-1815
2573-1815
DOI:10.1002/sscp.201800104