74209-46-4

Upstream product

• 64-17-5 ethanol 
• 22510-03-8 p-nitroacetophenoxime tosylate 
• 917-58-8 potassium ethoxide 
• 22510-03-8 p-Nitroacetophenonoxime tosylate 

Downstream Products

• 74209-48-6 2-(4-Aminophenyl)-2,2-diethoxyethylamine 
• 109564-92-3 (1S)-2-oxo-bornane-10-sulfonic acid-(4-nitro-phenacylamide) 
• 908007-34-1 [2-(4-acetylamino-phenyl)-2,2-diethoxy-ethyl]-carbamic acid benzyl ester 
• 908007-24-9 [5-(4-acetylamino-phenyl)-1H-imidazol-2-yl]-acetic acid ethyl ester 
• 908007-12-5 N-[4-(2-amino-1,1-diethoxy-ethyl)-phenyl]-acetamide 
• 908007-33-0 [2,2-diethoxy-2-(4-nitro-phenyl)-ethyl]-carbamic acid benzyl ester 
• 220444-96-2 7-chloro-1,9-bis-(4-nitro-phenyl)-4H-3,10,10a-triaza-benzo[f]azulene 

Relevant academic research and scientific papers

Efficient synthesis of 2-imidazol-2-ylacetates

A simple method of synthesizing various 2-imidazol-2-ylacetates is described. Condensation of α-aminoketals with imidates, followed by cyclization in refluxing 4 M-HCl/Dioxane, yielded 2-imidazol-2-ylacetates under one-pot and mild reaction conditions.