Preferential Crystallization of D, L-Pyridyl Alanine by Diastereoisomer Method
Since pyridyl alanine (PA) synthesized as an intermediate of medicine is racemic, the mixture requires optical separation. A novel method of optical separation comprising the formation of diastereoisomer salt by L-tartaric acid and preferential fractional crystallization was found, and the optical p...
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Veröffentlicht in: | KAGAKU KOGAKU RONBUNSHU 1991/03/10, Vol.17(2), pp.232-237 |
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Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng ; jpn |
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Online-Zugang: | Volltext |
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Zusammenfassung: | Since pyridyl alanine (PA) synthesized as an intermediate of medicine is racemic, the mixture requires optical separation. A novel method of optical separation comprising the formation of diastereoisomer salt by L-tartaric acid and preferential fractional crystallization was found, and the optical purity of L-PA crystals obtained was more than 96 %. Furthermore, it was clarified that the crystallization of D-PA, which is useless for medicine, is depressed by addition of NaOH to the crystallization solution. Finally, by using the Z-factor proposed by us as a key factor in crystallizer scale-up, the optimum design for industrial crystallization was developed. |
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ISSN: | 0386-216X 1349-9203 |
DOI: | 10.1252/kakoronbunshu.17.232 |