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L-酒石酸酯立体选择性萃取分离扁桃酸对映体 被引量:14

Enantioselective Separation of Racemic Mandelic Acid by Chiral Extraction with Lipophilic L-Tartaric Esters
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摘要 Distribution behavior of mandelic acid enantiomers was examined in a two-phase aqueous-organic solvent mixture containing L-tartaric esters. The influences of pH, length of alkyl chain of L-tartraic esters, organic solvents and concentrations of phosphate salt on partition coefficient(K) and separation factor(α) were investigated. The results show that L-tartaric esters studied all form more stable diastereomeric complexes with D-enantiomer than with L-enantiomer. With rise of pH, K decrease, but α increase. With addition of length of alkyl chain of L-tartaric esters, K and α decrease. Organic solvents and concentrations of phosphate salt also show a great influence on K and α. K L, K D and α are 2.523, 2.674 and 1.06, respectively, when mandelic acid enantiomers were extracted by di-O-pentyl-L-tartaric ester in n-decanol at pH=2.3. Distribution behavior of mandelic acid enantiomers was examined in a two-phase aqueous-organic solvent mixture containing L-tartaric esters. The influences of pH, length of alkyl chain of L-tartraic esters, organic solvents and concentrations of phosphate salt on partition coefficient(K) and separation factor(α) were investigated. The results show that L-tartaric esters studied all form more stable diastereomeric complexes with D-enantiomer than with L-enantiomer. With rise of pH, K decrease, but α increase. With addition of length of alkyl chain of L-tartaric esters, K and α decrease. Organic solvents and concentrations of phosphate salt also show a great influence on K and α. K L, K D and α are 2.523, 2.674 and 1.06, respectively, when mandelic acid enantiomers were extracted by di-O-pentyl-L-tartaric ester in n-decanol at pH=2.3.
出处 《应用化学》 CAS CSCD 北大核心 2003年第11期1108-1110,共3页 Chinese Journal of Applied Chemistry
基金 湖南省自然科学基金资助项目 ( 0 1JJY2 0 98)
关键词 扁桃酸对映体 L-酒石酸酯 手性萃取 分离 mandelic acid enantiomer,L-tartaric esters,chiral extraction,separation
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