76460-87-2

Basic information

• Product Name: 2-(1-Acetyl-pyrrolidin-2-yl)-1-phenyl-ethanone
• Synonyms: 2-(1-Acetyl-pyrrolidin-2-yl)-1-phenyl-ethanone
• CAS NO: 76460-87-2
• Molecular Weight: 231.294
• Mol File: 76460-87-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-(1-Acetyl-pyrrolidin-2-yl)-1-phenyl-ethanone(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(1-Acetyl-pyrrolidin-2-yl)-1-phenyl-ethanone(76460-87-2)
• EPA Substance Registry System: 2-(1-Acetyl-pyrrolidin-2-yl)-1-phenyl-ethanone(76460-87-2)

Safety Data

• Hazardous Substances Data: 76460-87-2(Hazardous Substances Data)

Upstream product

• 62024-31-1 1-phenyl-2-(pyrrolidin-2-yl)ethan-1-one 
• 108-24-7 acetic anhydride 
• 614-20-0 3-oxo-3-phenylpropionic acid 
• 4030-18-6 N-(acetyl)pyrrolidine 
• 621-82-9 Cinnamic acid 
• 94-02-0 ethyl 3-oxo-3-phenylpropionate 
• 13735-81-4 1-styrenyloxytrimethylsilane 
• 63050-21-5 N-acetyl-2-methoxypyrrolidine 

Relevant articles and documents

Nickel-catalyzed sp3 C-H bond activation from decarboxylative cross-coupling of α,β-unsaturated carboxylic acids with amides

Nickel-catalyzed functionalization of C(sp3)-H bonds adjacent to a nitrogen atom in amides through decarboxylative cross-coupling of α,β-unsaturated carboxylic acids is reported. A possible reaction mechanism is proposed that involves radical intermediate species. Georg Thieme Verlag Stuttgart, New York.

Electroorganic Chemistry. 46. A New Carbon-Carbon Bond Forming Reaction at the α-Position of Amines Utilizing Anodic Oxidation as a Key Step

A new carbon-carbon bond forming reaction at the α-position of primary and secondary amines has been exploited.The method involves anodic oxidation of urethanes derived from the primary and secondary amines and subsequent acid-catalyzed reaction of the re