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Towards a Scalable Synthesis of 2-Oxabicyclo[2.2.0]hex-5-en-3-one Using Flow Photochemistry.
Williams, Jason D; Otake, Yuma; Coussanes, Guilhem; Saridakis, Iakovos; Maulide, Nuno; Kappe, C Oliver.
Afiliación
  • Williams JD; Center for Continuous Flow Synthesis and Processing (CCFLOW) Research Center Pharmaceutical Engineering GmbH (RCPE) Inffeldgasse 13 8010 Graz Austria.
  • Otake Y; Institute of Chemistry University of Graz NAWI Graz Heinrichstrasse 28 8010 Graz Austria.
  • Coussanes G; Institute of Chemistry University of Graz NAWI Graz Heinrichstrasse 28 8010 Graz Austria.
  • Saridakis I; Present address: Laboratory for Chemistry and Life Science Institute of Innovative Research Tokyo Institute of Technology 4259 Nagatsuta-cho, Midori-ku Yokohama 226-8503 Japan.
  • Maulide N; Institute of Organic Chemistry University of Vienna Währinger Strasse 38 1090 Vienna Austria.
  • Kappe CO; Institute of Organic Chemistry University of Vienna Währinger Strasse 38 1090 Vienna Austria.
ChemPhotoChem ; 3(5): 229-232, 2019 May.
Article en En | MEDLINE | ID: mdl-31423462
Cyclobutene lactones hold great potential as synthetic building blocks, yet their preparation by photochemical rearrangement in batch can often be a bottleneck in synthetic studies. We report the use of flow photochemistry as a tool to enable a higher-throughput approach to the synthesis of 2-oxabicyclo[2.2.0]hex-5-en-3-one, which reduces reaction times from 24 h to 10 min. Accordingly, a significantly improved throughput of 144 mg/h (vs 14-21 mg/h in batch) was achieved. Scale-out experiments showed problematic reactor fouling and steps were taken to explore and minimize this effect.
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: ChemPhotoChem Año: 2019 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: ChemPhotoChem Año: 2019 Tipo del documento: Article