CuOTf(Tol)<sub>1/2</sub>-Catalyzed O-Trifluoroethylation of Alcohols with 2,2,2-Trifluorodiazoethane

Trifluoroethyl groups are important in medicinal chemistry since they can impart desirable properties, such as enhanced lipophilicity, metabolic stability, or binding affinity. A practical and scalable protocol has been developed for O-trifluoroethylation of alcohols with 2,2,2-trifluorodiazoethane using Cu(OTf)(Tol)<sub>1/2</sub> catalyst under mild conditions. This novel approach demonstrated high reactivity and broad substrate scope toward a diverse range of alcohols, ranging from fused and bridged ring systems, linear alcohols, to even sugar motifs, which makes the protocol valuable for medicinal chemistry, material science, and other areas where the introduction of trifluoroethyl groups would be beneficial.

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Publication Details

Journal
Organic Letters
Published
2025-04-21
DOI
https://doi.org/10.1021/acs.orglett.5c00942
Citations
1
Primary Topic
Fluorine in Organic Chemistry
Type
article
Field-Weighted Citation Impact
0.79
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CuOTf(Tol)1/2-Catalyzed O-Trifluoroethylation of Alcohols with 2,2,2-Trifluorodiazoethane

Zhiyu Lei, Xin Wen, Leyi Tao, Tao Ji et al.
1 citations
Organic Letters
Fluorine in Organic Chemistry
0.79
article

CuOTf(Tol)1/2-Catalyzed O-Trifluoroethylation of Alcohols with 2,2,2-Trifluorodiazoethane

Zhiyu Lei, Xin Wen, Leyi Tao, Tao Ji, James Roane, Yeon‐Hee Lim, Bin Hu, Lianyun Zhao
article en
1 citations

Abstract

Trifluoroethyl groups are important in medicinal chemistry since they can impart desirable properties, such as enhanced lipophilicity, metabolic stability, or binding affinity. A practical and scalable protocol has been developed for O-trifluoroethylation of alcohols with 2,2,2-trifluorodiazoethane using Cu(OTf)(Tol)<sub>1/2</sub> catalyst under mild conditions. This novel approach demonstrated high reactivity and broad substrate scope toward a diverse range of alcohols, ranging from fused and bridged ring systems, linear alcohols, to even sugar motifs, which makes the protocol valuable for medicinal chemistry, material science, and other areas where the introduction of trifluoroethyl groups would be beneficial.

Organic LettersVol. 27(17)
Merck & Co., Inc., Rahway, NJ, USA (United States) (US), WuXi AppTec (China) (CN), WuXi AppTec (United States) (US)
Clean water and sanitation
Openalex Percentile: Top 29%
Fluorine in Organic Chemistry
0.79
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