1285686-74-9

Upstream product

• 106-40-1 4-bromo-aniline 
• 122-39-4 diphenylamine 
• 36809-26-4 4-N,N-diphenylamino-1-bromobenzene 
• 589-87-7 1,4-bromoiodobenzene 
• 1285686-62-5 C₁₄H₁₅BrN₂O₂ 
• 201802-67-7 4-(diphenylamino)phenyl boronic acid 
• 1019056-21-3 dimethyl 4-(diphenylamino)phenylboronate 

Relevant academic research and scientific papers

Synthesis of triphenylamine-modified arylates and ketones via suzuki coupling reactions

A series of triphenylamine-mdified arylates and ketones were synthesized via Pd-catalyzed Suzuki coupling reaction of triphenylamine boronic acid with aryl bromide. The triphenylamine boronic acid was synthesized by iodization of 4-bromoaniline, Ullmann reaction of 1-bromo-4-iodobenzene with diphenylamine, and boronic acidification of 4-bromotriphenylamine.