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Fluorination of fatty alcohols with 1,1,2,3,3,3-hexafluoropropyl diethylamine

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Journal of the American Oil Chemists Society

Abstract

Fluorination of fatty alcohols with 1,1,2,3,3,3-hexafluoropropyl di-ethylamine (PPDA) was investigated. A mixture of lauryl fluoride (yield 45%) and lauryl 2,3,3,3-tetrafluoropropionate (yield 22%) was obtained from the reaction of PPDA and lauryl alcohol. Similar results were obtained from other fatty alcohols.

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References

  1. Sharts, CM., and W.A. Sheppard, Org. React. 21:158 (1974).

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  2. Takaoka, A., H. Iwakiri and N. Ishikawa, Bull. Chem. Soc. Jpn. 52:3377(1979).

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Watanabe, S., Fujita, T., Suga, K. et al. Fluorination of fatty alcohols with 1,1,2,3,3,3-hexafluoropropyl diethylamine. J Am Oil Chem Soc 60, 1678–1679 (1983). https://doi.org/10.1007/BF02662433

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  • DOI: https://doi.org/10.1007/BF02662433

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