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Multigram Synthesis of a Combustion‐Relevant δ‐Ketohydroperoxide through Sulfonylhydrazine Substitution

A synthesis of a δ‐ketohydroperoxide is described, addressing potential functional‐group compatibilities in these elusive species relevant to combustion and atmospheric chemistries. The hydroperoxide is installed via sulfonylhydrazine substitution, which was found to be more effective than displacem...

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Detalles Bibliográficos
Autores principales: Ke, Yan‐Ting, Gall, Bradley K., Dewey, Nicholas S., Rotavera, Brandon, Ferreira, Eric M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9643622/
https://www.ncbi.nlm.nih.gov/pubmed/35945143
http://dx.doi.org/10.1002/chem.202202266
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author Ke, Yan‐Ting
Gall, Bradley K.
Dewey, Nicholas S.
Rotavera, Brandon
Ferreira, Eric M.
author_facet Ke, Yan‐Ting
Gall, Bradley K.
Dewey, Nicholas S.
Rotavera, Brandon
Ferreira, Eric M.
author_sort Ke, Yan‐Ting
collection PubMed
description A synthesis of a δ‐ketohydroperoxide is described, addressing potential functional‐group compatibilities in these elusive species relevant to combustion and atmospheric chemistries. The hydroperoxide is installed via sulfonylhydrazine substitution, which was found to be more effective than displacement of secondary halides. As part of this protocol, it was observed that 1,2‐dimethoxyethane is an advantageous medium for the reaction, avoiding the formation of a tetrahydrofuran hydroperoxide side product. This discovery facilitated the multigram synthesis (6 steps, 41 % yield overall) and discrete characterization of the target δ‐ketohydroperoxide.
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spelling pubmed-96436222023-01-09 Multigram Synthesis of a Combustion‐Relevant δ‐Ketohydroperoxide through Sulfonylhydrazine Substitution Ke, Yan‐Ting Gall, Bradley K. Dewey, Nicholas S. Rotavera, Brandon Ferreira, Eric M. Chemistry Research Articles A synthesis of a δ‐ketohydroperoxide is described, addressing potential functional‐group compatibilities in these elusive species relevant to combustion and atmospheric chemistries. The hydroperoxide is installed via sulfonylhydrazine substitution, which was found to be more effective than displacement of secondary halides. As part of this protocol, it was observed that 1,2‐dimethoxyethane is an advantageous medium for the reaction, avoiding the formation of a tetrahydrofuran hydroperoxide side product. This discovery facilitated the multigram synthesis (6 steps, 41 % yield overall) and discrete characterization of the target δ‐ketohydroperoxide. John Wiley and Sons Inc. 2022-09-02 2022-11-07 /pmc/articles/PMC9643622/ /pubmed/35945143 http://dx.doi.org/10.1002/chem.202202266 Text en © 2022 The Authors. Chemistry - A European Journal published by Wiley-VCH GmbH https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Ke, Yan‐Ting
Gall, Bradley K.
Dewey, Nicholas S.
Rotavera, Brandon
Ferreira, Eric M.
Multigram Synthesis of a Combustion‐Relevant δ‐Ketohydroperoxide through Sulfonylhydrazine Substitution
title Multigram Synthesis of a Combustion‐Relevant δ‐Ketohydroperoxide through Sulfonylhydrazine Substitution
title_full Multigram Synthesis of a Combustion‐Relevant δ‐Ketohydroperoxide through Sulfonylhydrazine Substitution
title_fullStr Multigram Synthesis of a Combustion‐Relevant δ‐Ketohydroperoxide through Sulfonylhydrazine Substitution
title_full_unstemmed Multigram Synthesis of a Combustion‐Relevant δ‐Ketohydroperoxide through Sulfonylhydrazine Substitution
title_short Multigram Synthesis of a Combustion‐Relevant δ‐Ketohydroperoxide through Sulfonylhydrazine Substitution
title_sort multigram synthesis of a combustion‐relevant δ‐ketohydroperoxide through sulfonylhydrazine substitution
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9643622/
https://www.ncbi.nlm.nih.gov/pubmed/35945143
http://dx.doi.org/10.1002/chem.202202266
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