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Review
. 2013 Dec 5:9:2793-802.
doi: 10.3762/bjoc.9.314.

Flow microreactor synthesis in organo-fluorine chemistry

Affiliations
Review

Flow microreactor synthesis in organo-fluorine chemistry

Hideki Amii et al. Beilstein J Org Chem. .

Abstract

Organo-fluorine compounds are the substances of considerable interest in various industrial fields due to their unique physical and chemical properties. Despite increased demand in wide fields of science, synthesis of fluoro-organic compounds is still often faced with problems such as the difficulties in handling of fluorinating reagents and in controlling of chemical reactions. Recently, flow microreactor synthesis has emerged as a new methodology for producing chemical substances with high efficiency. This review outlines the successful examples of synthesis and reactions of fluorine-containing molecules by the use of flow microreactor systems to overcome long-standing problems in fluorine chemistry.

Keywords: defluorination; flow microreactor; fluorination; fluorine; organo-fluorine; perfluoroalkylation.

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Figures

Scheme 1
Scheme 1
Direct fluorination using microreactor systems.
Scheme 2
Scheme 2
Use of DAST in continuous-flow reactors.
Scheme 3
Scheme 3
Flow microreactor synthesis of fluorinated epoxides.
Scheme 4
Scheme 4
Highly controlled isomerization of gem-difluoroalkenes.
Scheme 5
Scheme 5
Flow system for catalytic aromatic fluorination.
Scheme 6
Scheme 6
Continuous-flow reactor for electrophilic aromatic fluorination.
Scheme 7
Scheme 7
Examples of [18F]-radiolabeled molecular imaging probes.
Scheme 8
Scheme 8
Flow microreactor synthesis of dipeptides.
Scheme 9
Scheme 9
Flow synthesis involving SNAr reactions.
Scheme 10
Scheme 10
Flow synthesis of fluoroquinolone antibiotics.
Scheme 11
Scheme 11
Highly controlled formation of PFPMgBr.
Scheme 12
Scheme 12
Selective flow synthesis of photochromic diarylethenes.
Scheme 13
Scheme 13
Flow microreactor system for perfluoroalkylation by generation of perfluoroalkyllithiums in the presence of electrophiles.
Scheme 14
Scheme 14
Integrated flow microreactor system for perfluoroalkylation by generation of perfluoroalkyllithiums in the absence of electrophiles.

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References

    1. Banks R E, Smart B E, Tatlow J C. Organofluorine Chemistry: Principles and Commercial Applications. New York: Plenum Press; 2000.
    1. Hiyama T, Kanie K, Kusumoto T, et al. Organofluorine Compounds: Chemistry and Application. Berlin: Springer-Verlag; 2000. - DOI
    1. Kirsch P. Modern Fluoroorganic Chemistry. Weinheim: Wiley-VCH; 2004. - DOI
    1. Chambers R D. Fluorine in Organic Chemistry. Oxford: Blackwell; 2004. - DOI
    1. Uneyama K. Organofluorine Chemistry. Oxford: Blackwell; 2006. - DOI