Enantioselective extraction of mandelic acid enantiomers by L-dipentyl tartrate and β-cyclodextrin as binary chiral selectors

Chemical Papers - Tập 61 - Trang 326-328 - 2007
F. P. Jiao1,2, X. Q. Chen1, W. G. Hu1, F. R. Ning1, K. L. Huang1
1School of Chemistry and Chemical Engineering, Central South University, Changsha, China
2School of Chemical Engineering, Xiangtan University, Xiangtan, China

Tóm tắt

A new binary chiral selector system effective for the enantioselective extraction of racemic mandelic acid is presented. While L-dipentyl tartrate and β-cyclodextrin had a very low enantioselectivity as single selectors, a preferential extraction of D-mandelic acid to the organic phase was found in the binary selector system. Using decanol as organic solvent and pH of a phoshate buffer equal to 2.3, the distribution coefficients of D-and L-mandelic acids as high as 14.9 and 7.0, respectively, and the enantioselectivity value of 2.1 were found at optimum concentration of β-cyclodextrin.

Tài liệu tham khảo

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