Enantioseparation of chiral mandelic acid derivatives by supercritical fluid chromatography

被引:12
作者
Ding, Jiawei [1 ]
Zhang, Ming [1 ]
Dai, Huixue [1 ]
Lin, Chunmian [1 ]
机构
[1] Zhejiang Univ Technol, Coll Environm, Hangzhou 310032, Zhejiang, Peoples R China
关键词
chiral; enantioseparation; mandelic acid; mobile phase additive; supercritical fluid chromatography; LIQUID-CHROMATOGRAPHY; MOBILE-PHASE; SEPARATION; POLYSACCHARIDE; AMYLOSE; CELLULOSE; POLYMER;
D O I
10.1002/chir.23018
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Mandelic acid and its derivatives are important chiral analogs which are widely used in the pharmaceutical synthetic industry. The present study investigated the enantiomeric separation of six mandelic acids (mandelic acid, 2-chloromandelic acid, 3-chloromandelic acid, 4-chloromandelic acid, 4-bromomandelic acid, 4-methoxymandelic acid) on the Chiralpak AD-3 column by supercritical fluid chromatography. The influences of volume fraction of trifluoroacetic acid, type and percentage of modifier, column temperature, and backpressure on the separation efficiency were investigated. And the enantiomer elution order was determined. The results show that, for a given modifier, the retention factor, the separation factor, and the separation resolution decreased gradually with increasing the volume ratio of the modifier. At the same volume ratio of modifier, the retention factor of the mandelic acid and its derivatives increased in the order of methanol, ethanol, and isopropanol, except 3-chloromandelic acid. The separation factor and the separation resolution decreased with the increase of column temperature (below the temperature limit). The backpressure affected the enantioseparation process: As the backpressure increased, a corresponding decrease in retention factor was observed. Under the same chiral column conditions, the SFC method exhibited faster and more efficient separation with better enantioselectivity than the HPLC method.
引用
收藏
页码:1245 / 1256
页数:12
相关论文
共 30 条
[21]  
[王转 Wang Zhuan], 2015, [药物分析杂志, Chinese Journal of Pharmaceutical Analysis], V35, P1127
[22]   Enantio separation of amino acid derivatives on an immobilized network polymer derived from L-tartaric acid [J].
Weng, W ;
Wang, QH ;
Yao, BX ;
Le Zeng, Q .
JOURNAL OF CHROMATOGRAPHY A, 2004, 1042 (1-2) :81-87
[23]   A comparison of HPLC and SFC chiral method development screening approaches for compounds of pharmaceutical interest [J].
Wong, Megan M. ;
Holzheuer, William B. ;
Webster, Gregory K. .
CURRENT PHARMACEUTICAL ANALYSIS, 2008, 4 (02) :101-105
[24]  
Xiao Q. B., 2012, SYNTHESIS CHIRAL AMI, P1
[25]   Structural analysis of amylose tris(3,5-dimethylphenylcarbamate) by NMR relevant to its chiral recognition mechanism in HPLC [J].
Yamamoto, C ;
Yashima, E ;
Okamoto, Y .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2002, 124 (42) :12583-12589
[26]   A facile light-emitting-diode induced fluorescence detector coupled to an integrated microfluidic device for microchip electrophoresis [J].
Yang, Fan ;
Li, Xin-chun ;
Zhang, Wen ;
Pan, Jian-bin ;
Chen, Zuan-guang .
TALANTA, 2011, 84 (04) :1099-1106
[27]   Comparative separation of chiral compounds by supercritical fluid chromatography and high performance liquid chromatography [J].
Zhang Jing ;
Chen Xiaodong ;
Li Liqun ;
He Jianfeng ;
Fan Jun ;
Zhang Weiguang .
CHINESE JOURNAL OF CHROMATOGRAPHY, 2016, 34 (03) :321-326
[28]  
Zhang N, 2002, CHINA CHEM IND NEWS, V2-21
[29]   Chiral separation of selected proline derivatives using a polysaccharide-type stationary phase by supercritical fluid chromatography and comparison with high-performance liquid chromatography [J].
Zhao, Yanqun ;
Pritts, Wayne A. ;
Zhang, Shuhong .
JOURNAL OF CHROMATOGRAPHY A, 2008, 1189 (1-2) :245-253
[30]  
[周丹 ZHOU Dan], 2006, [分析测试学报, Journal of Instrumental Analysis], V25, P49