93304-03-1

Basic information

• Product Name: Ethanone, 1-(1-methyl-1H-pyrrol-2-yl)-2-phenyl-
• CAS NO: 93304-03-1
• Molecular Formula: C13H13NO
• Molecular Weight: 199.252
• Mol File: 93304-03-1.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: Ethanone, 1-(1-methyl-1H-pyrrol-2-yl)-2-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-(1-methyl-1H-pyrrol-2-yl)-2-phenyl-(93304-03-1)
• EPA Substance Registry System: Ethanone, 1-(1-methyl-1H-pyrrol-2-yl)-2-phenyl-(93304-03-1)

Safety Data

• Hazardous Substances Data: 93304-03-1(Hazardous Substances Data)

Upstream product

• 96-54-8 N-Methylpyrrole 
• 140-29-4 phenylacetonitrile 
• 1085430-85-8 2-(1-methyl-1H-pyrrol-2-yl)-3-phenylpropanamide 
• 117068-07-2 α-(dimethylamino)-α-(1-methylpyrrol-2-yl)acetonitrile 
• 100-39-0 benzyl bromide 
• 103-80-0 phenylacetyl chloride 
• 26214-68-6 1-methyl-pyrrole-2-carboxylic acid chloride 
• 6973-60-0 1-Methyl-2-pyrrolecarboxylic acid 
• 591-50-4 iodobenzene 
• 34438-71-6 acetophenone enolate 
• 932-16-1 N-methyl-2-acetylpyrrole 
• 108-86-1 bromobenzene 
• 93303-99-2 <(1-methyl-2-pyrrolyl)carbonyl>trimethylsilane 

Downstream Products

• 86012-92-2 1-(1-Methyl-1H-pyrrol-2-yl)-2-phenylethanol 
• 126231-24-1 1-(5-Bromo-1-methyl-1H-pyrrol-2-yl)-2-phenyl-ethanone 
• 126231-26-3 1-(4-Bromo-1-methyl-1H-pyrrol-2-yl)-2-phenyl-ethanone 
• 126231-28-5 1-(4,5-Dibromo-1-methyl-1H-pyrrol-2-yl)-2-phenyl-ethanone 
• 126231-23-0 2-bromo-1-(1-methyl-1H-pyrrol-2-yl)-2-phenylethanone 
• 126231-27-4 2-Bromo-1-(4-bromo-1-methyl-1H-pyrrol-2-yl)-2-phenyl-ethanone 
• 126231-25-2 2-Bromo-1-(5-bromo-1-methyl-1H-pyrrol-2-yl)-2-phenyl-ethanone 
• 126231-29-6 2-Bromo-1-(4,5-dibromo-1-methyl-1H-pyrrol-2-yl)-2-phenyl-ethanone 
• 1338919-40-6 (2R)-2-(1-methyl-5-(phenylacetyl)-1H-pyrrol-3-yl)-2-hydroxyacetic acid n-butyl ester 

Relevant articles and documents

Acylation of pyrroles and their free (N-H)-derivatives via palladium-catalyzed carbopalladation of nitriles

An efficient regioselective synthesis of 2-acylpyrroles via palladium-catalyzed addition of pyrroles with benzonitriles and subsequent hydrolysis is developed. The direct acylation reaction of protected as well as (NH)-free pyrroles proceeded smoothly to

Unexpectedly high activity of Zn(OTf)2·6H2O in catalytic Friedel-Crafts acylation reaction

Zn(OTf)2·6H2O was used to promote Friedel-Crafts acylation of aromatics. The work describes the high activity and efficiency of Zn(OTf)2·6H2O in acylation of aromatics, and the catalyst has surpassed most metal triflates in dispensing when dried at high temperature under vacuum before use. Copyright Taylor & Francis Group, LLC.

Ytterbium (III) trifluoromethanesulfonate catalysed Friedel-Crafts acylation of 1-methylpyrrole in ionic liquid

In the presence of a catalytic amount of ytterbium (III) trifluoromethanesulfonate [Yb(OTf)3], 1-methylpyrrole can easily react with acyl chlorides in an ionic liquid [bpy][BF4](bpy=1- butylpyridine) to form corresponding ketones in satisfactory yield. The recyclability of the ionic liquid/catalyst system is demonstrated.