TY - JOUR
T1 - A Mathematically Simplified Solid-Solid-Liquid Ternary Phase Diagram with Tie-Lines for Early Process Development Validated by Chiral Resolution of Racemic Ibuprofen
AU - Pratama, Dhanang Edy
AU - Huang, Chia Yen
AU - Lee, Tu
N1 - Publisher Copyright:
© 2024 American Chemical Society.
PY - 2024/6/12
Y1 - 2024/6/12
N2 - Predictions of the purity and yield of a solid product by solid-liquid separation, such as reaction crystallization and extraction, can accurately be captured if the solid-solid-liquid ternary phase diagram of the product-impurity-solvent system is available. However, constructing the phase diagram with tie-lines experimentally is tedious, time-consuming, and unsuitable for solvent selection during early process development. In this work, a mathematical model for predicting the purity and yield of a given solvent was developed without the need to establish the full phase diagram. Just by determining a few vital points in the ternary phase diagram, we can rapidly predict the outcome for a given setting by computation, which can speed up the assessment of suitable solvent candidates for early process development significantly. This approach has been validated against the case of chiral resolution of racemic ibuprofen by diastereomeric salt formation with (S)-1-phenylethylamine.
AB - Predictions of the purity and yield of a solid product by solid-liquid separation, such as reaction crystallization and extraction, can accurately be captured if the solid-solid-liquid ternary phase diagram of the product-impurity-solvent system is available. However, constructing the phase diagram with tie-lines experimentally is tedious, time-consuming, and unsuitable for solvent selection during early process development. In this work, a mathematical model for predicting the purity and yield of a given solvent was developed without the need to establish the full phase diagram. Just by determining a few vital points in the ternary phase diagram, we can rapidly predict the outcome for a given setting by computation, which can speed up the assessment of suitable solvent candidates for early process development significantly. This approach has been validated against the case of chiral resolution of racemic ibuprofen by diastereomeric salt formation with (S)-1-phenylethylamine.
UR - http://www.scopus.com/inward/record.url?scp=85189988662&partnerID=8YFLogxK
U2 - 10.1021/acs.iecr.4c00442
DO - 10.1021/acs.iecr.4c00442
M3 - 期刊論文
AN - SCOPUS:85189988662
SN - 0888-5885
VL - 63
SP - 10397
EP - 10409
JO - Industrial and Engineering Chemistry Research
JF - Industrial and Engineering Chemistry Research
IS - 23
ER -