Reactions of 2-methoxy-3,3-dimethyl-2-phenyloxirane or α-bromoisobutyrophenone and carbon dioxide in the presence of aliphatic α,ω-diamines were investigated. 1,4-Butanediamine, 1,6-hexanediamine, 1,8-octanediamine, and 1,4-bis(aminomethyl)benzene afforded corresponding 3-(ω-aminoalkyl)-4-hydroxy-5,5-dimethyl-4-phenyl-2-oxazolidinones and 3,3′-polymethylenebis[4-hydroxy-5,5-dimethyl-4-phenyl-2-oxazolidinones] derivatives, while ethylenediamine gave only mono(2-oxazolidinone) derivative.
No takes yet. Share an insight, caveat, or question.
Saito et al. (1986) studied this question.
Synapse has enriched one closely related paper. Consider it for comparative context: