104226-37-1

Basic information

• Product Name: Benzenemethanamine, N-methyl-N-(4-nitrophenyl)-
• CAS NO: 104226-37-1
• Molecular Formula: C14H14N2O2
• Molecular Weight: 242.277
• Mol File: 104226-37-1.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: Benzenemethanamine, N-methyl-N-(4-nitrophenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanamine, N-methyl-N-(4-nitrophenyl)-(104226-37-1)
• EPA Substance Registry System: Benzenemethanamine, N-methyl-N-(4-nitrophenyl)-(104226-37-1)

Safety Data

• Hazardous Substances Data: 104226-37-1(Hazardous Substances Data)

Upstream product

• 614-30-2 N-methyl-N-phenyl-benzenemethanamine 
• 14309-92-3 N-benzyl-4-nitroaniline 
• 77-78-1 dimethyl sulfate 
• 108-88-3 toluene 
• 100-15-2 N-methyl(p-nitroaniline) 
• 905718-45-8 [(4-nitrophenyl)(phenyl)iodonium trifluoromethanesulfonate] 
• 103-67-3 benzyl-methyl-amine 
• 24067-17-2 4-nitrophenylboronic acid 
• 100-46-9 benzylamine 
• 100-00-5 4-chlorobenzonitrile 
• 636-98-6 p-nitrobenzene iodide 
• 586-78-7 para-nitrophenyl bromide 
• 7647-01-0 hydrogenchloride 
• 64-19-7 acetic acid 

Downstream Products

• 104226-31-5 N-benzyl-N-methyl-p-phenylenediamine 
• 13426-96-5 N-benzyl-N-methyl-2,4-dinitroaniline 
• 85046-51-1 N-nitroso N-benzyl-N-(4-nitroaniline) 

Relevant articles and documents

Regioselective nitration of N,N-dialkylanilines using cerium(IV) ammonium nitrate in acetonitrile

A highly regioselective and inexpensive nitration of N,N-dialkylanilines by cerium(IV) ammonium nitrate (CAN) in acetonitrile under room temperature to yield p-nitryl-N,N-dialkylanilines in good yields was reported.

Iron-Catalyzed Oxidative Amination of Benzylic C(sp3)–H Bonds with Anilines

Iron-catalyzed oxidative amination of benzylic C(sp3)–H bonds with anilines bearing electron-withdrawing groups (EWGs) or electron-donating groups (EDGs) is realized based on simple variations of N-substituents on imidazolium cations in novel ionic Fe(III) complexes. The structural modification of the imidazolium cation resulted in regulation of the redox potential and the catalytic performance of the iron metal center. Using DTBP as oxidant, [HItBu][FeBr4] showed the highest catalytic activity for anilines bearing EWGs, while [HIPym][FeBr4] was more efficient for EDG-substituted anilines. This work provides alternative access to benzylamines with the advantages of both a wide substrate scope and iron catalysis.

Application of ionic iron (III) complex as catalyst in preparation of benzylamine compound

The invention discloses the application of an ionic iron (III) complex as a catalyst in preparation of a benzylamine compound, that is, an ionic iron (III) complex having a formula of [(RNCHCHNR)CH][FeBr4] (R is tert-butyl) and containing 1,3-di-tert-butyl imidazolium cation is used as a catalyst, di-tert-butyl peroxide is used as an oxidizing agent, and a benzylamine compound is synthesized by oxidation reaction of a toluene/ethylbenzene compound with an aromatic amine. The application of an ionic iron (III) complex as a catalyst in preparation of a benzylamine compound has wide application range, and is applicable not only to a toluene compound containing a benzylic primary carbon-hydrogen bond but also to an ethylbenzene compound containing a benzyl secondary carbon-hydrogen bond. Thisis the first example of the preparation of a benzylamine compound by oxidation reaction of a toluene/ethylbenzene compound and an aromatic amine by an iron-based catalyst.