46727-16-6

Upstream product

• 95-78-3 2,5-Dimethylaniline 
• 100-51-6 benzyl alcohol 
• 100-52-7 benzaldehyde 
• 60669-05-8 N-sulphinyl-2,5-xylidine 

Downstream Products

• 5405-19-6 benzyl-(2,5-dimethylphenyl)amine 
• 16552-06-0 α-Cyan-zimtsaeure-<2,5-dimethyl-anilid> 
• 1206831-33-5 C₃₉H₄₃N₃ 
• 1206831-38-0 C₃₉H₄₁Cl₂HfN₃ 
• 1206831-37-9 C₃₉H₄₁Cl₂N₃Zr 
• 1697-13-8 3-(2,5-dimethyl-phenyl)-2-phenyl-2,3-dihydro-benzo[e][1,3]oxazin-4-one 
• 1697-22-9 3-(2,5-dimethyl-phenyl)-8-methyl-2-phenyl-2,3-dihydro-benzo[e][1,3]oxazin-4-one 
• 21354-48-3 2,5-dimethyl-N-methylaniline 

Relevant academic research and scientific papers

NaF regulated aqueous phase synthesis of aromatic amides and imines catalyzed by Au/HT

An Au/HT catalyst was found to be an efficient heterogeneous catalyst for the coupling reaction of aromatic alcohols and amines. The amides and imines can be selectively synthesized with up to 99% yield with or without the addition of NaF as the cocatalyst. This journal is the Partner Organisations 2014.

Proline triflate catalysed Diels-Alder reaction in the synthesis of tetrahydroquinoline derivatives

Proline triflate was found to catalyse efficiently the one-pot synthesis of 2H-pyranotetrahydroquinolines from aryl imines, and 3,4-dihydro-2H-pyran with high stereoselectivity. The aryl imines were formed in situ from aromatic amines and arylaldehydes.