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Selective hydroxylation of aryl iodides to produce phenols under mild conditions using a supported copper catalyst.

ABSTRACT: Owing to the high activity and low-cost, copper-based catalysts are promising candidates for transforming aromatic halides to yield phenols. In this work, we report the selective hydroxylation of aromatic iodides to produce phenols using an atomically dispersed copper catalyst (Cu-ZnO-ZrO₂) under mild reaction conditions. The reactions were conducted without the use of additional organic ligands, and the protection of an inert atmosphere environment is not required. The catalyst can be easily prepared, scalable, and is very efficient for a wide range of substrates. The catalytic reactions can be carried out with only 1.24 mol% Cu loading, which shows great potential in mass production.

SUBMITTER: Hao L

PROVIDER: S-EPMC9036948 | biostudies-literature | 2021 Jul

REPOSITORIES: biostudies-literature

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Selective hydroxylation of aryl iodides to produce phenols under mild conditions using a supported copper catalyst.

Hao Leiduan L Auni Anika A Ding Guodong G Li Xiaoyu X Xu Haiping H Li Tao T Zhang Qiang Q

RSC advances 20210721 41

Owing to the high activity and low-cost, copper-based catalysts are promising candidates for transforming aromatic halides to yield phenols. In this work, we report the selective hydroxylation of aromatic iodides to produce phenols using an atomically dispersed copper catalyst (Cu-ZnO-ZrO<sub>2</sub>) under mild reaction conditions. The reactions were conducted without the use of additional organic ligands, and the protection of an inert atmosphere environment is not required. The catalyst can b ...[more]

PMID: 35478897

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