Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1314269 | Journal of Fluorine Chemistry | 2010 | 4 Pages |
Abstract
Reactions of dialkyl ethers with either fluorine or Selectfluor™ led to the formation of unusual difluorinated polyether products in modest yields. A mechanism involving initial fluorination of the site adjacent to ether oxygen followed by elimination of hydrogen fluoride, reaction of the generated enol system with a further equivalent of fluorinating agent giving an oxonium system which reacts with water during aqueous work-up to lead eventually to the products observed, is suggested.
Graphical abstractReactions of dialkyl ethers with either fluorine or Selectfluor™ led to the formation of unusual difluorinated polyether products in modest yields.Figure optionsDownload full-size imageDownload as PowerPoint slide
Keywords
Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Richard D. Chambers, Takashi Okazoe, Graham Sandford, Emmanuelle Thomas, Jelena Trmcic,