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Optimization of the Conditions for Preparation of Silyl Derivatives of Phenylcarboxylic Acids in Diethyl and Methyl tert-Butyl Ethers

机译:在二乙基和甲基叔丁基醚中制备苯基羧酸的甲硅烷基衍生物的条件的优化

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摘要

In this work, the optimum conditions of derivatization of six phenylcarboxylic acids (sepsis biomarkers) in diethyl ether and methyl tert-butyl ether were selected. N,O-Bis(trimethylsilyl)trifluoroacetamide (BSTFA) was used as a silylating agent. The following conditions were chosen as optimum in terms of sensitivity of the silylating agent and its amount: 300 mu L of ether and 80 mu L of BSTFA, at which the derivatization yield of the studied compounds in model solutions was more than 70% in diethyl ether and more than 85% in methyl tert-butyl ether. The developed conditions will make it possible to increase the derivatization yield at various sample preparation procedures (liquid-liquid or solid-phase extraction) compared to the currently used conditions.
机译:在这项工作中,选择了在乙醚和甲基叔丁基醚中六种苯基羧酸(败血症生物标志物)衍生化的最佳条件。 N,O-双(三甲基甲硅烷基)三氟乙酰胺(BSTFA)用作甲硅烷基化剂。就硅烷化剂的敏感性及其用量而言,选择以下条件为最佳条件:300μL的醚和80μL的BSTFA,在该条件下,模型溶液中所研究化合物在二乙基溶液中的衍生化率超过70%醚和超过85%的甲基叔丁基醚。与目前使用的条件相比,开发的条件将有可能在各种样品制备程序(液-液相或固相萃取)下提高衍生化收率。

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