100520-89-6

Upstream product

• 124-09-4 1,6-Hexanediamine 
• 13694-96-7 2-methoxy-3,3-dimethyl-2-phenyl-oxirane 
• 201230-82-2 carbon monoxide 
• 373-44-4 1,8-diaminooctan 
• 539-48-0 p-xylylidenediamine 
• 107196-95-2 3-(8-amino)octyl-4-hydroxy-5,5-dimethyl-4-phenyl-2-oxazolidinone 
• 107-15-3 ethylenediamine 
• 110-60-1 1,4-diaminobutane 
• 10409-54-8 2-bromo-2-methyl-1-phenyl-propan-1-one 
• 67-56-1 methanol 

Downstream Products

• 7476-54-2 3,5-dinitro-benzoic acid-(2,2-dimethoxy-1,1-dimethyl-2-phenyl-ethyl ester) 
• 107520-40-1 3,5-dinitro-benzoic acid-(2-chloro-2-methoxy-1,1-dimethyl-2-phenyl-ethyl ester) 
• 7476-67-7 2-(3,5-dinitro-benzoyloxy)-2-methyl-1-phenyl-propan-1-one 
• 101792-14-7 4-nitro-benzoic acid-(2-chloro-2-methoxy-1,1-dimethyl-2-phenyl-ethyl ester) 
• 7476-43-9 4-nitro-benzoic acid-(2,2-dimethoxy-1,1-dimethyl-2-phenyl-ethyl ester) 

Relevant academic research and scientific papers

Formation of Bis(2-oxazolidinone) Derivatives by Reactions of Methoxy-3,3-dimethyl-2-phenyloxirane or α-Bromoisobutyrophenone with Carbon Dioxide and Aliphatic α,ο-Diamines

Reactions of 2-methoxy-3,3-dimethyl-2-phenyloxirane or α-bromoisobutyrophenone and carbon dioxide in the presence of aliphatic α,ο-diamines were investigated. 1,4-Butanediamine, 1,6-hexanediamine, 1,8-octanediamine, and 1,4-bis(aminomethyl)benzene afforded corresponding 3-(ο-aminoalkyl)-4-hydroxy-5,5-dimethyl-4-phenyl-2-oxazolidinones and 3,3'-polymethylenebis derivatives, while ethylene-diamine gave only mono-(2-oxazolidinone) derivative.