Design and operation of a filter reactor for continuous production of a selected pharmaceutical intermediate

被引:19
作者
Christensen, Kim Mueller [1 ]
Pedersen, Michael Jonch [1 ]
Dam-Johansen, Kim [1 ]
Holm, Thomas Lonberg [2 ]
Skovby, Tommy [2 ]
Kiil, Soren [1 ]
机构
[1] Tech Univ Denmark, Dept Chem & Biochem Engn, DK-2800 Lyngby, Denmark
[2] H Lundbeck & Co AS, DK-4500 Nykobing Sjaelland, Denmark
关键词
Pharmaceuticals; Chemical reactors; Continuous design; Grignard; Batch; Optimization; CONTINUOUS-FLOW REACTORS; MICROREACTOR TECHNOLOGY; REVOLUTION; INDUSTRY; BATCH; TOOL;
D O I
10.1016/j.ces.2011.12.002
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
A novel filter reactor system for continuous production of selected pharmaceutical intermediates is presented and experimentally verified. The filter reactor system consists of a mixed flow reactor equipped with a bottom filter, to retain solid reactant particles, followed by a conventional plug flow reactor, where residual reactant is converted by titration. A chemical case study, production of the pharmaceutical intermediate allylcarbinol by a reaction between allylmagnesium chloride and 2-chloro-thioxanthone, in the presence of a side reaction is considered. The synthesis is conducted in tetrahydrofuran solvent. The use of the filter reactor design was explored by examining the transferability of a synthesis step in a present full-scale semi-batch pharmaceutical production into continuous processing. The main advantages of the new continuous minireactor system, compared to the conventional semi-batch operation, are reduced impurity formation and the use of much lower reactor volumes (factor of 1000 based on the laboratory reactor) and less solvent consumption (from 5.8 to 2.3 L/kg reactant). Added challenges include handling of continuous solid powder feeding, stable pumping of reactive slurries, and a possibility of continuous control. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:111 / 117
页数:7
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