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A novel Tartaric acid derivative-based chiral resolving agent has been discovered for the enantiosepration of racemic Ibuprofen [(RS)-2-(4-(2-methyl propyl) phenyl) propanoic acid]. The processinvolves optimization of diastereomeric salt formed between (+) Ibuprofen and optically pure tartaric acid derivatives, followed by separating the individual enantiomer by acid salt preparation. Characterization of the synthesized compound has been carried out by elemental analysis, melting point, FT-IR, UV, HPLC, and 1H NMR spectra. The developed separation method is simple, cost-effective, and industrially viable.
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Jadhav et al. (2022) studied this question.
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