A NOVEL TECHNIQUE FOR THE PREPARATION OF SECONDARY FATTY AMIDES

A technique for the synthesis of monosubstituted fatty amides at low temperature and ambient pressure was developed. This method involved the condensation of an amine with a triacylglycerol. The primary amine (ethyl, n-butyl, n-hexyl and n-octyl were tested) acted as reagent and solvent for the fatty substrates. No additional organic solvent or catalyst was added. Tallow, vegetable oils and fish oil all served well as substrates, as did pure tripalmitin. The rate of amidation was dependent upon temperature and the ratio of fat to amine. In a series of experiments conducted with tallow and n-butylamine at a fat:amine molar ratio of 1:16, amidation could be carried out at 20-degrees-C, producing n-butyltallowamide in 83% yield in 24 hr. When the fat:amine molar ratio was reduced to 1:8, and the temperature raised to 45-degrees-C, the amide yield was 87.6% in 24 hr. When the reaction was carried out at the boiling point of n-butylamine (78-degrees-C) and at a fat:amine ratio of 1:8, the amide yield was 93.2% in 4 hr. The reaction progressed more rapidly with higher molecular weight amines. The identity and purity of the amides was assessed by thin-layer chromatography and confirmed by elemental analyses and infrared and C-13 nuclear magnetic resonance spectroscopy.