Suppr超能文献

超声辅助结晶法拆分四咪唑对映体在三元体系中与 O,O'-二苯甲酰基-(2R,3R)-酒石酸形成非对映异构体盐。

Effect of ultrasound-assisted crystallization in the diastereomeric salt resolution of tetramisole enantiomers in ternary system with O,O'-dibenzoyl-(2R,3R)-tartaric acid.

机构信息

Department of Organic Chemistry and Technology, Budapest University of Technology and Economics, 1521 Budapest, Hungary.

Department of Organic Chemistry and Technology, Budapest University of Technology and Economics, 1521 Budapest, Hungary.

出版信息

Ultrason Sonochem. 2016 Sep;32:8-17. doi: 10.1016/j.ultsonch.2016.02.015. Epub 2016 Feb 13.

Abstract

The diastereomeric salt resolution of racemic tetramisole was studied using ultrasound irradiation. We examined the effect of power and duration of ultrasonic irradiation on the properties of the crystalline phase formed by ultrasound-assisted crystallization and the result of the whole optical resolution. The results were compared with reference experiment without using ultrasound. The US time (5-30min) caused higher enantiomeric excess. Although yield was lower continuously high resolving efficiency could have been reached through ultrasound. We had the best results with 4.3W ultrasound power when resolvability was even higher than the best of reference. Furthermore, we accomplished a deep and thorough examination of the salts that possibly could form in this resolution. One of the four diastereomeric salts, which have been identified by powder X-ray diffraction, FTIR-spectroscopy, and differential scanning calorimetry (DSC) in the ternary system of the two tetramisole enantiomers and the resolving agent, namely the bis[(S)-tetramisole]-dibenzoyl-(R,R)-tartrate salt have been proven the key compound in the resolution process, and presented the highest melting point of 166°C (dec.) among the four salts. The originally expected diastereomeric bitartrate salts with 1:1M base:acid ratio [(S)-tetramisole-dibenzoyl-(R,R)-hydrogen-tartrate salt and (R)-tetramisole-dibenzoyl-(R,R)-hydrogen-tartrate salt] and their 'racemic' co-crystal [(RS)-tetramisole-dibenzoyl-(R,R)-hydrogen-tartrate salt] showed somewhat lower melting points (152, 145, and 150°C, respectively) and their crystallization was also prevented by application of ultrasound. Based on the melting points and enthalpies of fusion measured by DSC, all the binary and ternary phase diagrams have been newly established and calculated in the system with help of classical modelling equations of liquidus curves.

摘要

对消旋四咪唑的非对映异构体盐的拆分进行了超声辐射研究。我们考察了超声辐照功率和时间对超声辅助结晶形成的结晶相性质以及整个光学拆分结果的影响。将结果与未使用超声的参考实验进行了比较。超声时间(5-30min)导致对映体过量更高。虽然产率连续降低,但通过超声可以达到高的拆分效率。当超声功率为 4.3W 时,拆分效果甚至优于参考实验的最佳值,我们获得了最佳结果。此外,我们对可能在这种拆分中形成的盐进行了深入彻底的研究。在所研究的四元盐中,有一个通过粉末 X 射线衍射、FTIR 光谱和差示扫描量热法(DSC)在两种四咪唑对映体和拆分剂的三元体系中被鉴定出来,即双[(S)-四咪唑]-二苯甲酰基-(R,R)-酒石酸盐盐,它被证明是拆分过程中的关键化合物,其熔点最高,为 166°C(分解)。最初预期的 1:1M 碱基:酸比的非对映异构体酒石酸盐盐[(S)-四咪唑-二苯甲酰基-(R,R)-氢酒石酸盐盐和(R)-四咪唑-二苯甲酰基-(R,R)-氢酒石酸盐盐]及其“外消旋”共晶[(RS)-四咪唑-二苯甲酰基-(R,R)-氢酒石酸盐盐]的熔点较低(分别为 152、145 和 150°C),并且它们的结晶也被超声应用所阻止。基于 DSC 测量的熔点和熔融焓,在经典的液相曲线模型方程的帮助下,对系统中的所有二元和三元相图进行了重新建立和计算。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验