Triphenylphosphine/1,2-Diiodoethane-Promoted Formylation of Indoles with N,N-Dimethylformamide

Author:

Lin Jin-Hong12,Xiao Ji-Chang31,Zhu Yu-Rong31

Affiliation:

1. Key Laboratory of Organofluorine Chemistry, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Chinese Academy of Sciences (CAS)

2. Department of Chemistry, Innovative Drug Research Center, Shanghai University

3. College of Chemistry and Materials Science, Shanghai Normal University

Abstract

AbstractDespite intensive studies on the synthesis of 3-formylindoles, it is still highly desirable to develop efficient methods for the formylation of indoles, due to the shortcomings of the reported methods, such as inconvenient operations and/or harsh reaction conditions. Here, we describe a Ph3P/ICH2CH2I-promoted formylation of indoles with DMF under mild conditions. A Vilsmeier-type intermediate is readily formed from DMF promoted by the Ph3P/ICH2CH2I system. A one-step formylation process can be applied to various electron-rich indoles, but a hydrolysis needs to be carried out as a second step in the case of electron-deficient indoles. Convenient operations make this protocol attractive.

Funder

National Natural Science Foundation of China

Key Research Program of Frontier Science, Chinese Academy of Sciences

Publisher

Georg Thieme Verlag KG

Subject

Organic Chemistry

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