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http://dx.doi.org/10.5478/MSL.2020.11.4.103

Chiral Derivatization of Hydroxycarboxylic Acids Using 2,4,6-Trichlorobenzoyl Chloride as a Highly Efficient Regioselective Esterification Reagent for Gas Chromatography-Mass Spectrometry  

Park, Jeong Hyeok (Department of Chemistry, Gachon University)
Han, Sang Yun (Department of Chemistry, Gachon University)
Publication Information
Mass Spectrometry Letters / v.11, no.4, 2020 , pp. 103-107 More about this Journal
Abstract
We report the application of 2,4,6-trichlorobenzoyl chloride (often referred to as Yamaguchi esterification reagent) for the selective derivatization of the carboxylic group for GC-MS with the sample preparation method optimized for GC-MS analysis. The reagent was shown to be capable of selectively turning the carboxylic group into a reaction center, i.e., anhydride, of which the further reaction was directed to a near complete formation of required esters by unique steric and electronic effects of the reagent. Using the developed method, the chiral separation of hydroxycarboxylic acids by GC-MS using non-chiral columns was successfully demonstrated.
Keywords
2,4,6-trichlorobenzoyl chloride; chiral separation; GC-MS; hydroxycarboxylic acids; O-acetylated L-menthyl esters;
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