Direct C–H amination reactions of arenes with N-hydroxyphthalimides catalyzed by cuprous bromide

An efficient Cu-catalyzed strategy for the direct C–H amination of arenes in high yields using N-hydroxyphthalimide as the amidyl radical precursor under air is reported. A possible mechanism is proposed that proceeds via a radical reaction in the presence of CuBr and triethyl phosphite.

Bibliographic Details
Published in:Beilstein Journal of Organic Chemistry
Main Authors: Dongming Zhang, Bin Lv, Pan Gao, Xiaodong Jia, Yu Yuan
Format: Article
Language:English
Published: Beilstein-Institut 2022-06-01
Subjects:
Online Access:https://doi.org/10.3762/bjoc.18.65
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author Dongming Zhang
Bin Lv
Pan Gao
Xiaodong Jia
Yu Yuan
author_facet Dongming Zhang
Bin Lv
Pan Gao
Xiaodong Jia
Yu Yuan
author_sort Dongming Zhang
collection DOAJ
container_title Beilstein Journal of Organic Chemistry
description An efficient Cu-catalyzed strategy for the direct C–H amination of arenes in high yields using N-hydroxyphthalimide as the amidyl radical precursor under air is reported. A possible mechanism is proposed that proceeds via a radical reaction in the presence of CuBr and triethyl phosphite.
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spelling doaj-art-55d7dd16d10d4f09ba28fa916a2acaf42025-08-19T22:09:53ZengBeilstein-InstitutBeilstein Journal of Organic Chemistry1860-53972022-06-0118164765210.3762/bjoc.18.651860-5397-18-65Direct C–H amination reactions of arenes with N-hydroxyphthalimides catalyzed by cuprous bromideDongming Zhang0Bin Lv1Pan Gao2Xiaodong Jia3Yu Yuan4College of Chemistry and Chemical Engineering, Yangzhou University, Yangzhou 225002, P. R. of China College of Chemistry and Chemical Engineering, Yangzhou University, Yangzhou 225002, P. R. of China College of Chemistry and Chemical Engineering, Yangzhou University, Yangzhou 225002, P. R. of China College of Chemistry and Chemical Engineering, Yangzhou University, Yangzhou 225002, P. R. of China College of Chemistry and Chemical Engineering, Yangzhou University, Yangzhou 225002, P. R. of China An efficient Cu-catalyzed strategy for the direct C–H amination of arenes in high yields using N-hydroxyphthalimide as the amidyl radical precursor under air is reported. A possible mechanism is proposed that proceeds via a radical reaction in the presence of CuBr and triethyl phosphite.https://doi.org/10.3762/bjoc.18.65aminationcoppern-hydroxyphthalimidesradical reactionstriethyl phosphite
spellingShingle Dongming Zhang
Bin Lv
Pan Gao
Xiaodong Jia
Yu Yuan
Direct C–H amination reactions of arenes with N-hydroxyphthalimides catalyzed by cuprous bromide
amination
copper
n-hydroxyphthalimides
radical reactions
triethyl phosphite
title Direct C–H amination reactions of arenes with N-hydroxyphthalimides catalyzed by cuprous bromide
title_full Direct C–H amination reactions of arenes with N-hydroxyphthalimides catalyzed by cuprous bromide
title_fullStr Direct C–H amination reactions of arenes with N-hydroxyphthalimides catalyzed by cuprous bromide
title_full_unstemmed Direct C–H amination reactions of arenes with N-hydroxyphthalimides catalyzed by cuprous bromide
title_short Direct C–H amination reactions of arenes with N-hydroxyphthalimides catalyzed by cuprous bromide
title_sort direct c h amination reactions of arenes with n hydroxyphthalimides catalyzed by cuprous bromide
topic amination
copper
n-hydroxyphthalimides
radical reactions
triethyl phosphite
url https://doi.org/10.3762/bjoc.18.65
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