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Oxygenation of Phenols with Water as the Oxygen Source and Oxoammonium Salt as the Oxidant.
Wang, Yongtao; Liu, Jiaxin; Sun, Wenjing; Zhou, Yujia; Wang, Xinyu; Hu, Qixuan; Wen, Zeyu; Yao, Jia; Li, Haoran.
Afiliación
  • Wang Y; Department of Chemistry, Zhejiang University, 866 Yuhangtang Rd, Hangzhou 310058, China.
  • Liu J; Center of Chemistry for Frontier Technologies, ZJU-NHU United R&D Center, Zhejiang University, 866 Yuhangtang Rd, Hangzhou 310058, China.
  • Sun W; Department of Chemistry, Zhejiang University, 866 Yuhangtang Rd, Hangzhou 310058, China.
  • Zhou Y; Department of Chemistry, Zhejiang University, 866 Yuhangtang Rd, Hangzhou 310058, China.
  • Wang X; Department of Chemistry, Zhejiang University, 866 Yuhangtang Rd, Hangzhou 310058, China.
  • Hu Q; Department of Chemistry, Zhejiang University, 866 Yuhangtang Rd, Hangzhou 310058, China.
  • Wen Z; Department of Chemistry, Zhejiang University, 866 Yuhangtang Rd, Hangzhou 310058, China.
  • Yao J; Department of Chemistry, Zhejiang University, 866 Yuhangtang Rd, Hangzhou 310058, China.
  • Li H; Department of Chemistry, Zhejiang University, 866 Yuhangtang Rd, Hangzhou 310058, China.
J Org Chem ; 89(4): 2440-2447, 2024 Feb 16.
Article en En | MEDLINE | ID: mdl-38306296
ABSTRACT
Aromatic C-H oxygenation is important in both industrial production and organic synthesis. Here we report a metal-free approach for phenol oxygenation with water as the oxygen source using oxoammonium salts as the renewable oxidant. Employing this protocol, various alkyl-substituted phenols were converted into benzoquinones in yields of 59-98%. On the basis of 18O-labeling and kinetic studies, the hydroxy-oxoammonium adduct was proposed to attack the aromatic ring similarly to electrophilic aromatic substitution. We suppose that the findings described here not only provide an efficient and highly selective protocol for aromatic C-H oxygenation but also may encourage further developments of possible transition-metal-free catalytic methods.

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: J Org Chem Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: J Org Chem Año: 2024 Tipo del documento: Article País de afiliación: China