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The self–indicating preparation of bromoferrocenes from stannylferrocenes and an improved synthesis of di-iodoferrocene

A simple method for the preparation of bromoferrocenes from stannylferrocenes is described: the preparation of 1,1′-dibromoferrocene is used as an example. Stannylferrocenes are reacted with bromine directly in dichloromethane to give bromoferrocenes in a self-indicating titration reaction. Also, an...

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Autores principales: Butler, Ian R., Mehdar, Yassin T.H., Al-Taie, Zahraa S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7486603/
https://www.ncbi.nlm.nih.gov/pubmed/32954028
http://dx.doi.org/10.1016/j.heliyon.2020.e04824
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author Butler, Ian R.
Mehdar, Yassin T.H.
Al-Taie, Zahraa S.
author_facet Butler, Ian R.
Mehdar, Yassin T.H.
Al-Taie, Zahraa S.
author_sort Butler, Ian R.
collection PubMed
description A simple method for the preparation of bromoferrocenes from stannylferrocenes is described: the preparation of 1,1′-dibromoferrocene is used as an example. Stannylferrocenes are reacted with bromine directly in dichloromethane to give bromoferrocenes in a self-indicating titration reaction. Also, an enhanced method of removal of the highly soluble organotin tin by-products formed in the preparation of 1,1′-diiodoferrocene from 1,1′-tri-n-butylstannylferrocene is reported allowing the preparation of large-scale quantities of 1,1′-diiodoferrocene, which is one of the most important starting materials in ferrocene chemistry.
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spelling pubmed-74866032020-09-18 The self–indicating preparation of bromoferrocenes from stannylferrocenes and an improved synthesis of di-iodoferrocene Butler, Ian R. Mehdar, Yassin T.H. Al-Taie, Zahraa S. Heliyon Research Article A simple method for the preparation of bromoferrocenes from stannylferrocenes is described: the preparation of 1,1′-dibromoferrocene is used as an example. Stannylferrocenes are reacted with bromine directly in dichloromethane to give bromoferrocenes in a self-indicating titration reaction. Also, an enhanced method of removal of the highly soluble organotin tin by-products formed in the preparation of 1,1′-diiodoferrocene from 1,1′-tri-n-butylstannylferrocene is reported allowing the preparation of large-scale quantities of 1,1′-diiodoferrocene, which is one of the most important starting materials in ferrocene chemistry. Elsevier 2020-09-06 /pmc/articles/PMC7486603/ /pubmed/32954028 http://dx.doi.org/10.1016/j.heliyon.2020.e04824 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Butler, Ian R.
Mehdar, Yassin T.H.
Al-Taie, Zahraa S.
The self–indicating preparation of bromoferrocenes from stannylferrocenes and an improved synthesis of di-iodoferrocene
title The self–indicating preparation of bromoferrocenes from stannylferrocenes and an improved synthesis of di-iodoferrocene
title_full The self–indicating preparation of bromoferrocenes from stannylferrocenes and an improved synthesis of di-iodoferrocene
title_fullStr The self–indicating preparation of bromoferrocenes from stannylferrocenes and an improved synthesis of di-iodoferrocene
title_full_unstemmed The self–indicating preparation of bromoferrocenes from stannylferrocenes and an improved synthesis of di-iodoferrocene
title_short The self–indicating preparation of bromoferrocenes from stannylferrocenes and an improved synthesis of di-iodoferrocene
title_sort self–indicating preparation of bromoferrocenes from stannylferrocenes and an improved synthesis of di-iodoferrocene
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7486603/
https://www.ncbi.nlm.nih.gov/pubmed/32954028
http://dx.doi.org/10.1016/j.heliyon.2020.e04824
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