148491-07-0

Upstream product

• 585-79-5 m-nitrobromobenzene 
• 100-51-6 benzyl alcohol 

Downstream Products

• 871795-20-9 3-cyclopentyl-aniline hydrochloride 
• 91131-69-0 1-cyclopentyl-3-iodo-benzene 
• 94838-67-2 3-cyclopentyl-aniline 
• 1438900-62-9 N⁴,N⁴,N^4',N^4'-tetrabenzyl-2,2'-dibromo-[1,1'-biphenyl]-4,4'-diamine 
• 1394051-74-1 N,N-dibenzyl-3-(dimesitylboryl)aniline 
• 1394051-77-4 N-(3-dimesitylborylphenyl)-N’-methylimidazolium iodide 
• 1394051-76-3 N-(3-dimesitylborylphenyl)imidazole 
• 1394051-75-2 3-(dimesitylboryl)aniline 
• 1355025-60-3 N,N-dibenzyl-3-bromo-4-((triisopropylsilyl)ethynyl)aniline 
• 1345610-49-2 tert-butyl 4-(3-N,N-dibenzylaminophenyl)-4-hydroxypiperidine-1-carboxylate 
• 871795-19-6 N,N-dibenzyl-3-cyclopentyl-aniline 

Relevant academic research and scientific papers

Ruthenium-catalyzed tertiary amine formation from nitroarenes and alcohols

A highly selective ruthenium-catalyzed C-N bond formation was developed by using the hydrogen-borrowing strategy. Various tertiary amines were obtained efficiently from nitroarenes and primary alcohols. The reaction tolerates a wide range of functionalities. A tentative mechanism was proposed for this direct amination reaction of alcohols with nitroarenes.