Cargando…
Metal-Free Synthesis of Aryltriphenylphosphonium Bromides by the Reaction of Triphenylphosphine with Aryl Bromides in Refluxing Phenol
[Image: see text] A metal-free synthesis of aryltriphenylphosphonium bromides by the reaction of triphenylphosphine with aryl bromides in refluxing phenol is developed. This reaction tolerates hydroxymethyl, hydroxyphenyl, and carboxyl groups in aryl bromides, allowing to synthesize multifunctional...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2019
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6648432/ https://www.ncbi.nlm.nih.gov/pubmed/31459795 http://dx.doi.org/10.1021/acsomega.9b00568 |
_version_ | 1783437867332141056 |
---|---|
author | Huang, Wenhua Zhong, Chun-Hong |
author_facet | Huang, Wenhua Zhong, Chun-Hong |
author_sort | Huang, Wenhua |
collection | PubMed |
description | [Image: see text] A metal-free synthesis of aryltriphenylphosphonium bromides by the reaction of triphenylphosphine with aryl bromides in refluxing phenol is developed. This reaction tolerates hydroxymethyl, hydroxyphenyl, and carboxyl groups in aryl bromides, allowing to synthesize multifunctional aryltriphenylphosphonium bromides, from which facile access to multifunctional aryldiphenylphosphines and their oxides by hydrolysis and subsequent reduction is exemplified. A two-step addition–elimination mechanism, with the elimination step being a fast step, is also proposed. |
format | Online Article Text |
id | pubmed-6648432 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-66484322019-08-27 Metal-Free Synthesis of Aryltriphenylphosphonium Bromides by the Reaction of Triphenylphosphine with Aryl Bromides in Refluxing Phenol Huang, Wenhua Zhong, Chun-Hong ACS Omega [Image: see text] A metal-free synthesis of aryltriphenylphosphonium bromides by the reaction of triphenylphosphine with aryl bromides in refluxing phenol is developed. This reaction tolerates hydroxymethyl, hydroxyphenyl, and carboxyl groups in aryl bromides, allowing to synthesize multifunctional aryltriphenylphosphonium bromides, from which facile access to multifunctional aryldiphenylphosphines and their oxides by hydrolysis and subsequent reduction is exemplified. A two-step addition–elimination mechanism, with the elimination step being a fast step, is also proposed. American Chemical Society 2019-04-11 /pmc/articles/PMC6648432/ /pubmed/31459795 http://dx.doi.org/10.1021/acsomega.9b00568 Text en Copyright © 2019 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Huang, Wenhua Zhong, Chun-Hong Metal-Free Synthesis of Aryltriphenylphosphonium Bromides by the Reaction of Triphenylphosphine with Aryl Bromides in Refluxing Phenol |
title | Metal-Free Synthesis of Aryltriphenylphosphonium Bromides
by the Reaction of Triphenylphosphine with Aryl Bromides in Refluxing
Phenol |
title_full | Metal-Free Synthesis of Aryltriphenylphosphonium Bromides
by the Reaction of Triphenylphosphine with Aryl Bromides in Refluxing
Phenol |
title_fullStr | Metal-Free Synthesis of Aryltriphenylphosphonium Bromides
by the Reaction of Triphenylphosphine with Aryl Bromides in Refluxing
Phenol |
title_full_unstemmed | Metal-Free Synthesis of Aryltriphenylphosphonium Bromides
by the Reaction of Triphenylphosphine with Aryl Bromides in Refluxing
Phenol |
title_short | Metal-Free Synthesis of Aryltriphenylphosphonium Bromides
by the Reaction of Triphenylphosphine with Aryl Bromides in Refluxing
Phenol |
title_sort | metal-free synthesis of aryltriphenylphosphonium bromides
by the reaction of triphenylphosphine with aryl bromides in refluxing
phenol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6648432/ https://www.ncbi.nlm.nih.gov/pubmed/31459795 http://dx.doi.org/10.1021/acsomega.9b00568 |
work_keys_str_mv | AT huangwenhua metalfreesynthesisofaryltriphenylphosphoniumbromidesbythereactionoftriphenylphosphinewitharylbromidesinrefluxingphenol AT zhongchunhong metalfreesynthesisofaryltriphenylphosphoniumbromidesbythereactionoftriphenylphosphinewitharylbromidesinrefluxingphenol |