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Separation of mandelic acid and its derivatives with new immobilized cellulose chiral stationary phase

机译:新型固定化纤维素手性固定相分离扁桃酸及其衍生物

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摘要

A new liquid chromatographic method has been developed for the chiral separation of the enantiomers of mandelic acid and their derivatives 2-chloromandelic acid, 4-hydroxymandelic acid, 4-methoxymandelic acid, and 3,4,5-trismethoxymandelic acid. The enantiomers were separated by a CHIRALPAK® IC (250 mm×4.6 mm, 5 μm). Mandelic acid, 4-methoxymandelic acid, and 3,4,5-trismethoxymandelic acid were baseline resolved (resolution factor (R S)=2.21, R S=2.14, and R S=3.70, respectively). In contrast, the enantioselectivities between CHIRALPAK® IC and 2-chloromandelic acid and 4-hydroxymandelic acid investigated were low. By comparing the chromatographs of mandelic acid enantiomers and mandelic acid spiked with (R)-mandelic acid, it was determined that the first effluent was (R)-mandelic acid.
机译:已经开发出一种新的液相色谱方法,用于手性分离扁桃酸及其衍生物2-氯扁桃酸,4-羟基扁桃酸,4-甲氧基扁桃酸和3,4,5-三甲氧基扁桃酸的对映异构体。对映体通过CHIRALPAK IC(250mm×4.6mm,5μm)分离。将扁桃酸,4-甲氧基扁桃酸和3,4,5-三甲氧基扁桃酸进行基线拆分(拆分系数(R S)= 2.21,R S = 2.14和R S = 3.70)。相反,所研究的CHIRALPAK®IC与2-氯扁桃酸和4-羟基扁桃酸之间的对映选择性较低。通过比较扁桃酸对映体和掺有(R)-扁桃酸的扁桃酸的色谱图,可以确定第一个流出物是(R)-扁桃酸。

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