1236115-61-9

Basic information

• Product Name: ethyl 2-(1-acetyl-4,5-diphenyl-1H-pyrrol-2-yl)ethanoate
• Synonyms: ethyl 2-(1-acetyl-4,5-diphenyl-1H-pyrrol-2-yl)ethanoate
• CAS NO: 1236115-61-9
• Molecular Weight: 347.414
• Mol File: 1236115-61-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: ethyl 2-(1-acetyl-4,5-diphenyl-1H-pyrrol-2-yl)ethanoate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 2-(1-acetyl-4,5-diphenyl-1H-pyrrol-2-yl)ethanoate(1236115-61-9)
• EPA Substance Registry System: ethyl 2-(1-acetyl-4,5-diphenyl-1H-pyrrol-2-yl)ethanoate(1236115-61-9)

Safety Data

• Hazardous Substances Data: 1236115-61-9(Hazardous Substances Data)

Upstream product

• 23652-56-4 ethyl (Z/E)-β-acetylaminobut-2-enoate 
• 501-65-5 diphenyl acetylene 

Relevant articles and documents

Pyrrole synthesis via allylic sp3 C-H activation of enamines followed by intermolecular coupling with unactivated alkynes

A conceptually novel pyrrole synthesis is reported, efficiently merging enamines and (unactivated) alkynes under oxidative conditions. In an intermolecular Rh catalyzed process, the challenging allylic sp3 C-H activation of the enamine substrates is followed by the cyclization with the alkyne (R3 = CO2R). Alternatively, in some cases (R 3 = CN), the enamine can be utilized for a vinylic sp2 C-H activation. A total of 17 examples with yields above 60% is presented, together with the results of an initial mechanistic investigation.