346720-43-2

Basic information

• Product Name: N-cyclopentyl-4-methoxybenzamide
• Synonyms: N-cyclopentyl-4-methoxybenzamide
• CAS NO: 346720-43-2
• Molecular Weight: 219.283
• Mol File: 346720-43-2.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: N-cyclopentyl-4-methoxybenzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-cyclopentyl-4-methoxybenzamide(346720-43-2)
• EPA Substance Registry System: N-cyclopentyl-4-methoxybenzamide(346720-43-2)

Safety Data

• Hazardous Substances Data: 346720-43-2(Hazardous Substances Data)

Upstream product

• 100-07-2 4-methoxy-benzoyl chloride 
• 1003-03-8 Cyclopentamine 
• 5614-37-9 cyclopentyl methyl ether 
• 874-90-8 4-methoxybenzonitrile 
• 933-05-1 cyclopentyl acetate 
• 930-28-9 cyclopentyl chloride 
• 201230-82-2 carbon monoxide 
• 19501-58-7 4-methoxyphenylhydrazine hydrochloride 
• 104-93-8 p-methylanizole 
• 15226-74-1 dicobalt octacarbonyl 
• 696-62-8 para-iodoanisole 
• 13939-06-5 molybdenum hexacarbonyl 

Relevant articles and documents

An efficient transformation of methyl ethers and nitriles to amides catalyzed by Iron(III) perchlorate hydrate

An efficient and inexpensive synthesis of N-substituted amides from the reaction of nitriles with methyl ethers catalyzed by Fe(ClO4)3·H2O is described. Fe(ClO4)3·H2O is an economically efficient catalyst for the Ritter Reaction under solvent-free conditions. A range of methyl ethers (benzyl, sec-alkyl and tert-butyl ethers) were reacted with nitriles to provide the corresponding amides in high–excellent yields.

FeCl2·4H2O catalyzed ritter reaction with nitriles and halohydrocarbons

An efficient and inexpensive synthesis of N-substituted amides from the Ritter reaction of nitriles with various halohydrocarbons catalyzed by FeCl2·4H2O is described. FeCl2·4H2O economically efficiently catalyzed the Ritter reaction under solvent-free conditions. A range of halohydrocarbons (benzyl, tert-butyl and sec-alkyl halohydrocarbons) were coupled with nitriles to provide the corresponding amides in high to excellent yields.

Convenient synthesis of amides by Zn(ClO4)2·6H2O catalysed Ritter reaction with nitriles and halohydrocarbons

A convenient and high yielding procedure for the synthesis of amides by the Ritter reaction of nitriles and halohydrocarbons in the presence of Zn(ClO4)2·6H2O as a highly stable, effective and available catalyst is described.