Synthesis of Trifluoromethylphosphines from Alkylphosphines

Abstract Despite their value as unique ligands, synthesizing trifluoromethylphosphines (TFMPhos) traditionally requires reactive precursors (bearing P–H, P–X, or P–Si bonds). Directly converting a P–C(sp3) into a P–CF3 bond remains a formidable challenge. Herein, we report a practical, transition-metal-free method for the direct conversion of alkylphosphines into TFMPhos using Togni’s reagent II and NaI. This operationally simple, mild protocol features broad functional group tolerance, providing versatile access to diverse TFMPhos derivatives.

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Publication Details

Journal
Organic Letters
Published
2026-10-15
DOI
https://doi.org/10.1021/acs.orglett.6c03969
Primary Topic
Organophosphorus compounds synthesis
Type
article
Field-Weighted Citation Impact
0.00

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article

Synthesis of Trifluoromethylphosphines from Alkylphosphines

Hongtai Chen, Longhui Chen, Guangwei Wang, Yingfan Yang et al.
Organic Letters
Organophosphorus compounds synthesis
article

Synthesis of Trifluoromethylphosphines from Alkylphosphines

Hongtai Chen, Longhui Chen, Guangwei Wang, Yingfan Yang, Jinwei Zhang
article en

Abstract

Abstract Despite their value as unique ligands, synthesizing trifluoromethylphosphines (TFMPhos) traditionally requires reactive precursors (bearing P–H, P–X, or P–Si bonds). Directly converting a P–C(sp3) into a P–CF3 bond remains a formidable challenge. Herein, we report a practical, transition-metal-free method for the direct conversion of alkylphosphines into TFMPhos using Togni’s reagent II and NaI. This operationally simple, mild protocol features broad functional group tolerance, providing versatile access to diverse TFMPhos derivatives.

Organic Letters
Tianjin University (CN), Tianjin Chengjian University (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 25%
Organophosphorus compounds synthesis
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