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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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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. |
format | Online Article Text |
id | pubmed-6686974 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
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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