98132-94-6

Basic information

• Product Name: diethyl-(4-butoxy-benzyl)-amine
• Synonyms: diethyl-(4-butoxy-benzyl)-amine
• CAS NO: 98132-94-6
• Molecular Weight: 235.37
• Mol File: 98132-94-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: diethyl-(4-butoxy-benzyl)-amine(CAS DataBase Reference)
• NIST Chemistry Reference: diethyl-(4-butoxy-benzyl)-amine(98132-94-6)
• EPA Substance Registry System: diethyl-(4-butoxy-benzyl)-amine(98132-94-6)

Safety Data

• Hazardous Substances Data: 98132-94-6(Hazardous Substances Data)

Upstream product

• 109-65-9 1-bromo-butane 
• 24619-86-1 4-((diethylamino)methyl)phenol 
• 23014-31-5 ethyl-(4-butoxy-benzyl)-amine 
• 75-03-6 ethyl iodide 
• 109-89-7 diethylamine 
• 40141-13-7 1-butoxy-4-(chloromethyl)benzene 
• 5736-88-9 p-butoxybenzaldehyde 
• 80-40-0 ethyl ester of p-toluenesulfonic acid 
• 6214-45-5 (4-butoxyphenyl)methanol 
• 24932-54-5 N,N-diethyl-4-methoxy-benzenemethanamine 
• 123-08-0 4-hydroxy-benzaldehyde 

Relevant articles and documents

Novel N-heterocyclic carbene cyclic palladium compound as well as preparation method and application thereof

The invention discloses a novel N-heterocyclic carbene cyclic palladium compound as well as a preparation method and application thereof, and belongs to the technical field of organic catalysis. The novel N-heterocyclic carbene cyclic palladium compound is prepared by the following steps: heating, stirring and mixing N-(4-butoxybenzyl)-N-ethylethylamine, palladium chloride and an organic solvent in an inert gas atmosphere, then adding potassium carbonate, performing stirring and mixing, and finally adding 1-(2,6-diisopropyl phenyl)-3-butyl-brominated imidazole for reflux reaction; and after the reaction is finished, performing quenching with an acid solution, performing extracting to obtain a crude product, and performing column chromatography separation and purification to obtain the novel N-heterocyclic carbene cyclic palladium compound. The N-heterocyclic carbene cyclic palladium compound provided by the invention has high catalytic activity, can catalyze cross-coupling reactions between aryl chloride and aryl phenylboronic acid and between aryl chloride and secondary amine in a catalytic amount of 1 mol%, and can be used as a high-efficiency catalyst for the coupling reactions.