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TMSCF3 as a Convenient Source of CF2=CF2 for Pentafluoroethylation, (Aryloxy)tetrafluoroethylation, and Tetrafluoroethylation

  • Lingchun Li
  • , Chuanfa Ni
  • , Qiqiang Xie
  • , Mingyou Hu
  • , Fei Wang
  • , Jinbo Hu
  • CAS - Shanghai Institute of Organic Chemistry

Research output: Contribution to journalArticlepeer-review

101 Scopus citations

Abstract

A new method for the on-site preparation of tetrafluoroethylene (TFE) and a procedure for its efficient use in pentafluoroethylation by fluoride addition were developed by using a simple two-chamber system. The on-site preparation of TFE was accomplished by dimerization of difluorocarbene derived from (trifluoromethyl)trimethylsilane (TMSCF3) under mild conditions. Other fluoroalkylation reactions, such as (aryloxy)tetrafluoroethylation and tetrafluoroethylation processes, were also achieved using a similar approach. This work not only demonstrates a convenient and safe approach for the generation and use of TFE in academic laboratories, but also provides a new strategy for pentafluoroethylation.

Original languageEnglish
Pages (from-to)9971-9975
Number of pages5
JournalAngewandte Chemie - International Edition
Volume56
Issue number33
DOIs
StatePublished - 7 Aug 2017
Externally publishedYes

Keywords

  • copper
  • difluorocarbene
  • pentafluoroethylation
  • tetrafluoroethylation
  • tetrafluoroethylene

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