We thank the Max-Planck Society and AstraZeneca UK for generous financial support. F.L. is the recipient of a postdoctoral fellowship from Fonds québécois de la recherche sur la nature et les technologies (FQRNT).
Communication
Continuous Synthesis and Purification by Direct Coupling of a Flow Reactor with Simulated Moving-Bed Chromatography†
Article first published online: 6 JUN 2012
DOI: 10.1002/anie.201202795
Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Additional Information
How to Cite
O'Brien, A. G., Horváth, Z., Lévesque, F., Lee, J. W., Seidel-Morgenstern, A. and Seeberger, P. H. (2012), Continuous Synthesis and Purification by Direct Coupling of a Flow Reactor with Simulated Moving-Bed Chromatography . Angew. Chem. Int. Ed., 51: 7028–7030. doi: 10.1002/anie.201202795
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Publication History
- Issue published online: 4 JUL 2012
- Article first published online: 6 JUN 2012
- Manuscript Received: 11 APR 2012
Funded by
- Max-Planck Society
- AstraZeneca UK
- Fonds québécois de la recherche sur la nature et les technologies (FQRNT)
Keywords:
- continuous synthesis;
- flow chemistry;
- nucleophilic aromatic substitution;
- purification;
- simulated moving-bed chromatography
Continuous synthesis meets continuous purification to produce pure products from crude reaction mixtures. In the nucleophilic aromatic substitution of 2,4-difluoronitrobenzene with morpholine the desired monosubstituted product can be continuously separated from the byproducts in a purity of over 99 % by coupling a flow reactor to a simulated moving bed (SMB) chromatography module (see scheme).

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