128037-41-2Relevant academic research and scientific papers
An efficient method for hydrolysis of N-monosubstituted amides utilization of intramolecular N---O acyl migration in hydroxypivalimides
Tsunoda, Tetsuto,Sasaki, Osamu,Takeuchi, Osamu,Ito, Sho
, p. 3925 - 3934 (2007/10/02)
An efficient and versatile method for the hydrolysis of N-monosubstituted carboxamides has been developed. The method consists of two steps: the conversion to acetoxypivalimides (≥90% yield) and their mild alkaline hydrolysis (70 90% yield). No epimerization at the α-position of the acyl group took place in the process. The amine part of the original amides can be recovered in good yield.
AN EFFICIENT METHOD FOR HYDROLYSIS OF N-MONOSUBSTITUTED AMIDES VIA ACETOXYPIVALIMIDES
Tsunoda, Tetsuto,Sasaki, Osamu,Ito, Sho
, p. 731 - 734 (2007/10/02)
Various N-monosubstituted carboxamides were efficiently hydrolyzed in two steps through acetoxypivalimides.The method can be applied to a wide range of amides without racemization of α-position of the acyl groups.The amines can also be recovered.
