Synthesis of Perfluorinated Ethers by Solution Phase Direct Fluorination: An Adaptation of the La-Mar Technique

Abstract

The synthesis of several perfluorinated ethers of pentaerythritol, dipentaerythritol, and tripentaerythritol by direct fluorination in solution is described. These ethers were perfluorinated using elemental fluorine in a two step process. In the first step, up to 95 percent of the hydrogens were replaced by fluorine while the ether was dissolved in a chlorofluorocarbon solvent. The remaining hydrogens were replaced by exposing the partially fluorinated product of pure fluorine at elevated temperature. Thesis.

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Document Details

Document Type
Technical Report
Publication Date
Aug 22, 1990
Accession Number
ADA225512

Entities

People

  • Gordon B. Rutherford

Organizations

  • University of Texas at Austin

Tags

Communities of Interest

  • Advanced Electronics
  • Biomedical
  • C4I

DTIC Thesaurus Topics

  • Alkanes
  • Boiling Point
  • Carbon Tetrachloride
  • Chemical Reaction Properties
  • Chemical Synthesis
  • Chemistry
  • Ethers
  • Fluorides
  • Fluorination
  • Fluorine
  • Fluorine Compounds
  • Hydrocarbon Fuels
  • Mass Spectra
  • Materials
  • Organic Chemistry
  • Organic Compounds
  • United States

Fields of Study

  • Chemistry

Readers

  • Analytical Chemistry
  • Organic Chemistry