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Synthesis of Aryl Iodides from Arylhydrazines and Iodine
[Image: see text] A metal- and base-free method is developed for the synthesis of aryl iodides from arylhydrazine hydrochlorides and iodine. A wide variety of aryl iodides can be conveniently synthesized by an equimolar reaction of arylhydrazine hydrochlorides and I(2) in dimethyl sulfoxide at 60 °C...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6645010/ https://www.ncbi.nlm.nih.gov/pubmed/31459110 http://dx.doi.org/10.1021/acsomega.8b01559 |
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author | Dong, Chun-ping Nakamura, Kentaro Taniguchi, Toshihide Mita, Soichiro Kodama, Shintaro Kawaguchi, Shin-ichi Nomoto, Akihiro Ogawa, Akiya Mizuno, Takumi |
author_facet | Dong, Chun-ping Nakamura, Kentaro Taniguchi, Toshihide Mita, Soichiro Kodama, Shintaro Kawaguchi, Shin-ichi Nomoto, Akihiro Ogawa, Akiya Mizuno, Takumi |
author_sort | Dong, Chun-ping |
collection | PubMed |
description | [Image: see text] A metal- and base-free method is developed for the synthesis of aryl iodides from arylhydrazine hydrochlorides and iodine. A wide variety of aryl iodides can be conveniently synthesized by an equimolar reaction of arylhydrazine hydrochlorides and I(2) in dimethyl sulfoxide at 60 °C for 6 h. In the iodination step, arylhydrazines are oxidized by iodine to form arenediazonium salts, which undergo single-electron transfer from iodide anion to give aryl and iodine radicals; subsequent combination of them affords the corresponding aryl iodides. |
format | Online Article Text |
id | pubmed-6645010 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-66450102019-08-27 Synthesis of Aryl Iodides from Arylhydrazines and Iodine Dong, Chun-ping Nakamura, Kentaro Taniguchi, Toshihide Mita, Soichiro Kodama, Shintaro Kawaguchi, Shin-ichi Nomoto, Akihiro Ogawa, Akiya Mizuno, Takumi ACS Omega [Image: see text] A metal- and base-free method is developed for the synthesis of aryl iodides from arylhydrazine hydrochlorides and iodine. A wide variety of aryl iodides can be conveniently synthesized by an equimolar reaction of arylhydrazine hydrochlorides and I(2) in dimethyl sulfoxide at 60 °C for 6 h. In the iodination step, arylhydrazines are oxidized by iodine to form arenediazonium salts, which undergo single-electron transfer from iodide anion to give aryl and iodine radicals; subsequent combination of them affords the corresponding aryl iodides. American Chemical Society 2018-08-23 /pmc/articles/PMC6645010/ /pubmed/31459110 http://dx.doi.org/10.1021/acsomega.8b01559 Text en Copyright © 2018 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 | Dong, Chun-ping Nakamura, Kentaro Taniguchi, Toshihide Mita, Soichiro Kodama, Shintaro Kawaguchi, Shin-ichi Nomoto, Akihiro Ogawa, Akiya Mizuno, Takumi Synthesis of Aryl Iodides from Arylhydrazines and Iodine |
title | Synthesis of Aryl Iodides from Arylhydrazines and Iodine |
title_full | Synthesis of Aryl Iodides from Arylhydrazines and Iodine |
title_fullStr | Synthesis of Aryl Iodides from Arylhydrazines and Iodine |
title_full_unstemmed | Synthesis of Aryl Iodides from Arylhydrazines and Iodine |
title_short | Synthesis of Aryl Iodides from Arylhydrazines and Iodine |
title_sort | synthesis of aryl iodides from arylhydrazines and iodine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6645010/ https://www.ncbi.nlm.nih.gov/pubmed/31459110 http://dx.doi.org/10.1021/acsomega.8b01559 |
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