15437-13-5

Usage

InChI:InChI=1/C15H15NO2/c1-2-18-14-10-8-12(9-11-14)15(17)16-13-6-4-3-5-7-13/h3-11H,2H2,1H3,(H,16,17)

Upstream product

• 103-71-9 phenyl isocyanate 
• 103-73-1 Phenetole 
• 99358-57-3 4-ethoxy benzoyl azide 
• 62-53-3 aniline 
• 7446-70-0 aluminium trichloride 
• 7719-09-7 thionyl chloride 
• 60-29-7 diethyl ether 
• 92850-70-9 4-ethoxy-benzophenone-seqtrans-oxime 
• 92850-70-9 4-ethoxy-benzophenone-seqcis-oxime 
• 619-86-3 4-(ethoxy)benzoic acid 
• 142-04-1 aniline hydrochloride 
• 349109-74-6 C₁₅H₁₄ClNO₂ 
• 1373758-57-6 C₁₀H₉NO₄ 
• 98-80-6 phenylboronic acid 

Relevant academic research and scientific papers

Visible-Light-Promoted Iron-Catalyzed N-Arylation of Dioxazolones with Arylboronic Acids

A visible-light-promoted and simple iron salt-catalyzed N-arylation was achieved efficiently under external photosensitizer-free conditions. Arylboronic acids and bench-stable dioxazolones were used for this cross-coupling reaction. This reaction features high reactivity, wide substrate scope, good functional group tolerance, simple operation procedure, and mild reaction conditions. Preliminary mechanistic investigations were conducted to support a radical pathway. This method may contribute to shift the paradigm of iron-catalyzed C-N bond construction and nitrene transfer chemistry.

Exploration of Cu-catalyzed regioselective hydrodehalogenation of o-haloanilides using EtOH as hydrogen source

In present work, we have explored a Cu(acac)2/vasicine-catalyzed regioselective hydrodehalogenation methodology of o-haloanilides using EtOH as hydrogen source and solvent. The catalytic system could selectively dehalogenate 2-Br and 2-I, and features regioselective, efficient and functional group tolerance.

Efficient Pd-Catalyzed Hydrodehalogenation of o -Haloanilides in Water

In the present work, we have developed a practical methodology for the hydrodehalogenation of o -haloanilides using PdCl 2at 100 °C under mild conditions in water. The catalytic system could selectively dehalogenate both aryl chloride and aryl bromide and exhibit a broad functional group tolerance.

Efficient method for the direct preparation of amides from carboxylic acids using tosyl chloride under solvent-free conditions

A simple, clean and highly efficient solvent-free procedure for the preparation of primary, secondary, tertiary and aromatic amides is described from the direct reaction of carboxylic acids and silica-supported ammonium salts, triethylamine (TEA) and tosyl chloride (TsCl) as condensing agent. The reaction proceeds rapidly in high yields at room temperature.