932252-71-6

Basic information

• Product Name: 3-(4-(tert-butyl)phenyl)-N,N-dimethylpropanamide
• Synonyms: 3-(4-(tert-butyl)phenyl)-N,N-dimethylpropanamide
• CAS NO: 932252-71-6
• Molecular Weight: 233.354
• Mol File: 932252-71-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 3-(4-(tert-butyl)phenyl)-N,N-dimethylpropanamide(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(4-(tert-butyl)phenyl)-N,N-dimethylpropanamide(932252-71-6)
• EPA Substance Registry System: 3-(4-(tert-butyl)phenyl)-N,N-dimethylpropanamide(932252-71-6)

Safety Data

• Hazardous Substances Data: 932252-71-6(Hazardous Substances Data)

Upstream product

• 201230-82-2 carbon monoxide 
• 1746-23-2 4-tert-Butylstyrene 
• 68-12-2 N,N-dimethyl-formamide 
• 127-19-5 N,N-dimethyl acetamide 
• 877-65-6 p-tert-butylbenzyl alcohol 

Relevant articles and documents

A highly efficient catalytic α-alkylation of unactivated amides using primary alcohols

The α-alkylation of unactivated amides with alcohols is described. Using a NCP-type pincer Ir complex as the precatalyst and KOtBu as the base, the reactions of secondary or tertiary acetamides with benzyl or nonbenzyl primary alcohols occur at 80 °C, furnishing the alkylation products in good yields. This method represents a practical and green means of α-alkylation of amides in a relatively mild, efficient, and selective manner with low catalyst loadings (0.5 mol %).

Palladium-Catalyzed Hydrocarbonylative C-N Coupling of Alkenes with Amides

An efficient palladium-catalyzed hydrocarbonylative C-N coupling of alkenes with amides has been developed. The reaction was performed via hydrocarbonylation of alkenes, followed by acyl metathesis with amides. Both intermolecular and intramolecular react