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毛细管气相色谱法分离2-苯基羧酸酯对映体
引用本文:史雪岩,刘飞鹏,边庆花.毛细管气相色谱法分离2-苯基羧酸酯对映体[J].色谱,2016,34(1):85-88.
作者姓名:史雪岩  刘飞鹏  边庆花
作者单位:1. 中国农业大学农学与生物技术学院, 北京 100193; 2. 中国农业大学理学院, 北京 100193
基金项目:公益性行业(农业)科技专项(201303027).
摘    要:手性2-芳基羧酸酯是制备手性非甾体抗炎药物2-芳基羧酸的重要的中间体,为了建立可用于2-苯基羧酸酯对映体分离的手性毛细管气相色谱法(CGC),分别使用2,6-二-O-戊基-3-O-丁酰基-β-环糊精及2,6-二-O-苄基-3-O-庚酰基-β-环糊精作毛细管气相色谱手性固定相,研究了其对2-苯基丁酸甲酯、2-苯基丁酸乙酯、2-苯基丁酸异丙酯、2-苯基丙酸甲酯及2-苯基丙酸环戊酯等5种2-苯基羧酸酯对映体的分离能力。结果表明,用2,6-二-O-戊基-3-O-丁酰基-β-环糊精及2,6-二-O-苄基-3-O-庚酰基-β-环糊精作手性固定相的毛细管气相色谱法可以分离2-苯基丁酸甲酯、2-苯基丙酸甲酯和2-苯基丙酸环戊酯对映体。2,6-二-O-戊基-3-O-丁酰基-β-环糊精对3种2-苯基羧酸酯对映体的分离能力超过了2,6-二-O-苄基-3-O-庚酰基-β-环糊精。

关 键 词:-环糊精衍生物  &beta  2-苯基羧酸酯  对映体分离  毛细管气相色谱  手性固定相  
收稿时间:2015-06-24

Enantioseparation of 2-phenylcarboxylic acid esters by capillary gas chromatography
SHI Xueyan,LIU Feipeng,BIAN Qinghua.Enantioseparation of 2-phenylcarboxylic acid esters by capillary gas chromatography[J].Chinese Journal of Chromatography,2016,34(1):85-88.
Authors:SHI Xueyan  LIU Feipeng  BIAN Qinghua
Institution:1. College of Agronomy and Biotechnology, China Agricultural University, Beijing 100193, China; 2. College of Science, China Agricultural University, Beijing 100193, China
Abstract:Chiral 2-arylcarboxylic acid derivatives are important intermediates for preparing 2-arylcarboxylic acids, which are non-steroidal anti-inflammatory drugs (NSAIDs). In order to separate 2-phenylcarboxylic acid ester enantiomers by capillary gas chromatography (CGC), 2,6-di-O-pentyl-3-O-butyryl- β-cyclodextrin and 2,6-di-O-benzyl-3-O-heptanoyl- β-cyclodextrin were used as CGC chiral stationary phases, separately, and their enantioseparation abilities to enantiomers of methyl 2-phenylbutanoate, ethyl 2-phenylbutanoate, isopropyl 2-phenylbutanoate, methyl 2-phenylpropionate and cyclopentyl 2-phenylpropionate were examined. It was found that methyl 2-phenylbutanoate, methyl 2-phenylpropionate and cyclopentyl 2-phenylpropionate were successfully separated by using 2,6-di-O-pentyl-3-O-butyryl- β-cyclodextrin and 2,6-di-O-benzyl-3-O-heptanoyl- β-cyclodextrin as CGC chiral stationary phases, respectively. The enantiomer separation abilities of 2,6-di-O-pentyl-3-O-butyryl- β-cyclodextrin to the three pairs of 2-phenylcarboxylic acid esters tested are superior to those of 2,6-di-O-benzyl-3-O-heptanoyl- β-cyclodextrin.
Keywords:β-cyclodextrin derivatives  2-phenylcarboxylic acid esters  capillary gas chromatography (CGC)  chiral stationary phases  enantiomer separation  
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