Synthesis, identification, chiral separation and crystal structure of (3R,4R,7S,8S)-3,4,7,8-tetrachlorodecane and its stereoisomers
Solveig Valderhaug,
Natalie Paškanová,
Jiří Tůma,
Jana Herciková,
Václav Eigner,
Huiling Liu,
Alexey Gorovoy,
Jon Eigill Johansen,
Odd Reidar Gautun
Affiliations
Solveig Valderhaug
Department of Chemistry, Norwegian University of Science and Technology (NTNU), Høgskoleringen 5, NO-7491, Trondheim, Norway; Chiron AS, Stiklestadveien 1, NO-7041 Trondheim, Norway
Natalie Paškanová
Department of Organic Chemistry, University of Chemistry and Technology, Technická 5, 16628, Prague, Czech Republic
Jiří Tůma
Chiron AS, Stiklestadveien 1, NO-7041 Trondheim, Norway; Department of Organic Chemistry, University of Chemistry and Technology, Technická 5, 16628, Prague, Czech Republic
Jana Herciková
Department of Organic Chemistry, University of Chemistry and Technology, Technická 5, 16628, Prague, Czech Republic
Václav Eigner
Department of Solid State Chemistry, University of Chemistry and Technology, Technická 5, 16628, Prague, Czech Republic
Chlorinated paraffins (CPs) are a notoriously known class of compounds that stand amongst the most wide-spread persistent organic pollutants. Therefore, their reliable, repeatable, and reproducible quantitative analysis using well-defined reference standards is of utmost importance. In view of the increasing demand for constitutionally and stereochemically defined CP standards, we have synthesized a stereoisomeric mixture of 3,4,7,8-tetrachlorodecane. One stereoisomer – (3R,4R,7S,8S)-3,4,7,8-tetrachlorodecane was separated from the mixture, and enriched fractions of residual stereoisomers were achieved through crystallisation of the residual mother liquors. The molecular structure of the single isolated stereoisomer was confirmed through single-crystal X-ray crystallographic data. One fraction of 3,4,7,8-tetrachlorodecane stereoisomers was successfully separated on a chiral stationary phase using supercritical fluid chromatography hyphenated to mass spectrometry (column: Chiral ART Amylose-C; mobile phase: CO2/MeOH (96/4 v/v) with 0.1% diethylamine). The reported separation of stereoisomers is unprecedented in CP analysis so far.
