26923-87-5Relevant academic research and scientific papers
SYNTHESIS OF STERICALLY HINDERED SECONDARY AMINOETHER ALCOHOLS
-
Page/Page column 18, (2008/06/13)
Severely sterically hindered secondary aminoether alcohols are prepared by reacting organic carboxylic, organic carboxylic acid halides, acid anhydrides or a ketene with an alkyl, alkaryl or alkylhalo sulfonate to yield a sulfonic. Carboxylic anhydride compound which is then reacted with a dioxane to cleave the ring of the dioxane, yielding a cleavage product which cleavage product is then aminated with an alkylamine and hydrolyzed with base to yield the severely sterically hindered secondary aminoether alcohol.
