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Towards a Scalable Synthesis of 2‐Oxabicyclo[2.2.0]hex‐5‐en‐3‐one Using Flow Photochemistry

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‐oxabic...

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Autores principales: Williams, Jason D., Otake, Yuma, Coussanes, Guilhem, Saridakis, Iakovos, Maulide, Nuno, Kappe, C. Oliver
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6686974/
https://www.ncbi.nlm.nih.gov/pubmed/31423462
http://dx.doi.org/10.1002/cptc.201900017
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author Williams, Jason D.
Otake, Yuma
Coussanes, Guilhem
Saridakis, Iakovos
Maulide, Nuno
Kappe, C. Oliver
author_facet Williams, Jason D.
Otake, Yuma
Coussanes, Guilhem
Saridakis, Iakovos
Maulide, Nuno
Kappe, C. Oliver
author_sort Williams, Jason D.
collection PubMed
description 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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spelling pubmed-66869742019-08-14 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 ChemPhotoChem Communications 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. John Wiley and Sons Inc. 2019-02-18 2019-05 /pmc/articles/PMC6686974/ /pubmed/31423462 http://dx.doi.org/10.1002/cptc.201900017 Text en © 2019 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Communications
Williams, Jason D.
Otake, Yuma
Coussanes, Guilhem
Saridakis, Iakovos
Maulide, Nuno
Kappe, C. Oliver
Towards a Scalable Synthesis of 2‐Oxabicyclo[2.2.0]hex‐5‐en‐3‐one Using Flow Photochemistry
title Towards a Scalable Synthesis of 2‐Oxabicyclo[2.2.0]hex‐5‐en‐3‐one Using Flow Photochemistry
title_full Towards a Scalable Synthesis of 2‐Oxabicyclo[2.2.0]hex‐5‐en‐3‐one Using Flow Photochemistry
title_fullStr Towards a Scalable Synthesis of 2‐Oxabicyclo[2.2.0]hex‐5‐en‐3‐one Using Flow Photochemistry
title_full_unstemmed Towards a Scalable Synthesis of 2‐Oxabicyclo[2.2.0]hex‐5‐en‐3‐one Using Flow Photochemistry
title_short Towards a Scalable Synthesis of 2‐Oxabicyclo[2.2.0]hex‐5‐en‐3‐one Using Flow Photochemistry
title_sort towards a scalable synthesis of 2‐oxabicyclo[2.2.0]hex‐5‐en‐3‐one using flow photochemistry
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6686974/
https://www.ncbi.nlm.nih.gov/pubmed/31423462
http://dx.doi.org/10.1002/cptc.201900017
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