Copper(I) Iodide-Catalyzed Perfluoroalkoxylation Reaction of Alkyl Halides

We report an efficient perfluoroalkoxylation reaction of alkyl halides catalyzed by copper(I) iodide (CuI), which facilitates the simultaneous activation of both perfluoroalkoxide and alkyl halides. This methodology is tolerant of a wide range of functional groups and eliminates the need for costly metal reagents. The reaction is conducted in a single step under mildly practical conditions.

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Publication Details

Journal
Organic Letters
Published
2024-08-15
DOI
https://doi.org/10.1021/acs.orglett.4c02428
Citations
3
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
0.62

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article

Copper(I) Iodide-Catalyzed Perfluoroalkoxylation Reaction of Alkyl Halides

Fanhong Wu, Wangchuan Xiao, Bingjun Le, Jingjing Wu et al.
3 citations
Organic Letters
Fluorine in Organic Chemistry
0.62
article

Copper(I) Iodide-Catalyzed Perfluoroalkoxylation Reaction of Alkyl Halides

Fanhong Wu, Wangchuan Xiao, Bingjun Le, Jingjing Wu, Chao Liu, Xiaoyu Ma, Xiong Wu
article en
3 citations

Abstract

We report an efficient perfluoroalkoxylation reaction of alkyl halides catalyzed by copper(I) iodide (CuI), which facilitates the simultaneous activation of both perfluoroalkoxide and alkyl halides. This methodology is tolerant of a wide range of functional groups and eliminates the need for costly metal reagents. The reaction is conducted in a single step under mildly practical conditions.

Organic LettersVol. 26(34)
Jingdong (China) (CN), Shanghai Institute of Organic Chemistry (CN), University of Chinese Academy of Sciences (CN), Shanghai Institute of Technology (CN)
National Natural Science Foundation of China, Science and Technology Commission of Shanghai Municipality, Shanghai Institute of Technology
Clean water and sanitation
Openalex Percentile: Top 37%
Fluorine in Organic Chemistry
0.62
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