One general application of trifluoroacetaldehyde is the preparation of trifluoroethylamino derivatives via reductive amination reaction. This synthesis includes the formation of the corresponding N,O-acetal intermediates followed by their reduction using NaBH4 or 2-picoline borane complex, affording the target trifluoroethylamino compounds in moderate to good yields. Another general application of trifluoroacetaldehyde is the synthesis of chiral α-substituted trifluoroethylamino compounds.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
One general application of trifluoroacetaldehyde is the preparation of trifluoroethylamino derivatives via reductive amination reaction. This synthesis includes the formation of the corresponding N,O-acetal intermediates followed by their reduction using NaBH4 or 2-picoline borane complex, affording the target trifluoroethylamino compounds in moderate to good yields. Another general application of trifluoroacetaldehyde is the synthesis of chiral α-substituted trifluoroethylamino compounds.
Solubility
Soluble in water.
Notes
Store at room temperature. Incompatible with oxidizing agents. Keep in cool place.
RUO – Research Use Only
General References:
- G. K. Surya Prakash.; Zhe Zhang.; Fang Wang.; Socrates Munoz.; George A. Olah. Nucleophilic Trifluoromethylation of Carbonyl Compounds: Trifluoroacetaldehyde Hydrate as a Trifluoromethyl Source.J. Org. Chem. 2013, 78 (7),3300-3305 .
- Mauno M. Airaksinen.; Per H. Rosenberg.; Tapani Tammisto. A Possible Mechanism of Toxicity of Trifluoroethanol and Other Halothane Metabolites.Acta Pharmacologica et Toxicologica. 1970, 28 (4),299-304 .