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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...

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Autores principales: Dong, Chun-ping, Nakamura, Kentaro, Taniguchi, Toshihide, Mita, Soichiro, Kodama, Shintaro, Kawaguchi, Shin-ichi, Nomoto, Akihiro, Ogawa, Akiya, Mizuno, Takumi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2018
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.
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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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