Ethyl trifluoroacetate explained

Ethyl trifluoroacetate is a chemical compound from the trifluoroacetate group.

Production

Ethyl trifluoroacetate can be obtained by reacting 2,4,6-tris-(trifluoromethyl)-1,3,5-triazine with ethanol in the presence of hydrochloric acid. The former, in turn, can be prepared by a two-step reaction starting from trichloroacetonitrile by reaction with hydrogen chloride and fluorination of the intermediate with antimony trifluoride.[1]

The compound can also be obtained by reacting trifluoroacetic acid or sodium trifluoroacetate[2] with ethanol.[3]

Properties

Ethyl trifluoroacetate is a colorless and odorless liquid that is sparingly soluble in water but miscible with chloroform and methanol. The compound exists in the gas phase in two more conformal forms.[4]

Use

Ethyl trifluoroacetate is used as an intermediate in organic synthesis to prepare organic fluorine compounds such as 3-ethyl-1-methylimidazolium trifluoroacetate (EMITA). It is also used in the synthesis of various pharmaceutically active molecules and agricultural products, and is also useful for the preparation of trifluoroacetylated compounds. The trifluoroacetyl group is widely used as an amine protecting group in organic synthesis because it can be easily removed under mild conditions.[5]

Notes and References

  1. T. R. Norton. Journal of the American Chemical Society. A New Synthesis of Ethyl Trifluoroacetate. 72. 8. 3527–3528. 0002-7863. 1950. 10.1021/ja01164a056.
  2. Book: R. L.. Murray. J. H.. Babcock. The Preparation of Sodium Trifluoroacetate and Ethyl Trifluoroacetate. Atomic Energy Commission. 1946.
  3. Google Patents: US4879407A - Process for the preparation of ethyl trifluoroacetate - Google Patents, retrieved 7 August 2022
  4. Journal of Raman Spectroscopy. Experimental and theoretical structure and vibrational analysis of ethyl trifluoroacetate, CF3CO2CH2CH3: Structure and vibrational analysis of CF3CO2CH2CH3. 41. 10. 1357–1368. 2010. 10.1002/jrs.2550.
  5. Tetrahedron Letters. Ethyl trifluoroacetate: a powerful reagent for differentiating amino groups. 36. 41. 7357–7360. 0040-4039. 1995. German. 10.1016/0040-4039(95)01655-4. Xu . Daqiang . Prasad . Kapa . Repic . Oljan . Blacklock . Thomas J. .