4171-11-3

Usage

InChI:InChI=1/C15H11NO3/c17-13-15(19-14(18)16-13,11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10H,(H,16,17,18)

Upstream product

• 57-13-6 urea 
• 52182-15-7 ethyl benzilate 
• 51-79-6 urethane 
• 598-50-5 N-Methylurea 
• 71-43-2 benzene 
• 2902-98-9 2-chloro-2,2-diphenylacetyl chloride 
• 4746-87-6 benzilamide 
• 105-58-8 Diethyl carbonate 
• 79458-02-9 (2,4-Dioxo-5,5-diphenyl-3-oxazolidinyl)carbamidsaeure-ethylester 
• 3019-71-4 Trichloroacetyl isocyanate 

Downstream Products

• 5841-23-6 3-methyl-5,5-diphenyl-oxazolidine-2,4-dione 
• 101890-47-5 3-butyl-5,5-diphenyl-oxazolidine-2,4-dione 
• 50484-25-8 3-ethyl-5,5-diphenyl-oxazolidine-2,4-dione 
• 54743-16-7 3-(2-dimethylamino-ethyl)-5,5-diphenyl-oxazolidine-2,4-dione 
• 74529-60-5 3-(4'-Carboxy-phenylsulfonyl)-5,5-diphenyl-2,4-oxazolidinedione 
• 74529-63-8 4-(2,4-Dioxo-5,5-diphenyl-oxazolidine-3-sulfonyl)-benzamide 
• 74529-65-0 5,5-Diphenyl-3-(3-trifluoromethyl-benzenesulfonyl)-oxazolidine-2,4-dione 
• 74529-64-9 3-(3-Acetyl-benzenesulfonyl)-5,5-diphenyl-oxazolidine-2,4-dione 
• 74529-59-2 4-(2,4-Dioxo-5,5-diphenyl-oxazolidine-3-sulfonyl)-benzoic acid ethyl ester 
• 131842-42-7 5-(Dimethylamino)-3,4-dihydro-3-(2-hydroxy-2,2-diphenylacetyl)-4-isopropyl-4-methyl-2H-imidazol-2-on 
• 131842-41-6 5-(Dimethylamino)-3,4-dihydro-3-(2-hydroxy-2,2-diphenylacetyl)-4,4-dimethyl-2H-imidazol-2-on 
• 74529-66-1 3-Benzoyl-5,5-diphenyl-oxazolidine-2,4-dione 
• 74529-68-3 3-(4-Methoxy-benzoyl)-5,5-diphenyl-oxazolidine-2,4-dione 
• 74529-67-2 3-(4-Nitro-benzoyl)-5,5-diphenyl-oxazolidine-2,4-dione 

Relevant academic research and scientific papers

A facile one-pot synthesis of 3-unsubstituted-2,4-oxazolidinediones via in situ generation of carbamates from α-hydroxyesters using trichloroacetyl isocyanate

A convenient, high yield one-pot methodology for the synthesis of pharmaceutically interesting 3-unsubstituted-2,4-oxazolidinediones from α-hydroxyesters is described. A primary carbamate was generated in situ from the corresponding α-hydroxyester and tri

Azomethine Imines by Reaction of Diphenylketene with Azodicarboxylates

The reaction of diphenylketene with azodicarboxylates yields azomethine imines 4 which show 1,3-dipolaric reactivity: addition of diphenylketene yields the 2:1 adduct 8, addition of phenylisocyanate productes 7, and dimerization leads to 5.