Benzenemethanamine, N-methyl-N-(4-methylphenyl)-

Base Information

• Chemical Name: Benzenemethanamine, N-methyl-N-(4-methylphenyl)-
• CAS No.: 69267-39-6
• Molecular Formula: C15H17N
• Molecular Weight: 211.307
• DSSTox Substance ID: DTXSID10449264
• Nikkaji Number: J473.829B
• Wikidata: Q82268678

Synonyms:N-benzyl-N,4-dimethylaniline;Benzenemethanamine, N-methyl-N-(4-methylphenyl)-;69267-39-6;benzyl-methyl-(p-tolyl)-amine;SCHEMBL8228982;DTXSID10449264

Chemical Property of Benzenemethanamine, N-methyl-N-(4-methylphenyl)-

Chemical Property:

• XLogP3: 4.6
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 3
• Exact Mass: 211.136099547
• Heavy Atom Count: 16
• Complexity: 188

Purity/Quality:

85.0-99.8% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=CC=C(C=C1)N(C)CC2=CC=CC=C2

Technology Process of Benzenemethanamine, N-methyl-N-(4-methylphenyl)-

There total 26 articles about Benzenemethanamine, N-methyl-N-(4-methylphenyl)- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 99.0%

para-chlorotoluene (106-43-4) + benzyl-methyl-amine (103-67-3) → N-benzyl-N-methyl-4-methylaniline (69267-39-6)

Guidance literature:

With C₃₅H₄₄Cl₂N₄Pd; potassium tert-butylate; In tetrahydrofuran; at 130 ℃; for 12h; Inert atmosphere; Sealed tube;

DOI:10.1039/c6ra02556k

Reference yield: 93.0%

N-methyl-N-(4-methylphenyl)benzamide (57212-26-7) → N-benzyl-N-methyl-4-methylaniline (69267-39-6)

Guidance literature:

With 1,1,3,3-Tetramethyldisiloxane; In ethyl acetate; at 20 - 80 ℃; for 10h; Green chemistry;

DOI:10.1002/adsc.201900838

Reference yield: 92.0%

N-benzyl-N-methyl-p-toluidine-N-oxide (19689-35-1) → N-benzyl-N-methyl-4-methylaniline (69267-39-6)

Guidance literature:

With phenylboronic acid; In dichloromethane; at 20 ℃; for 0.5h;

DOI:10.1016/j.tetlet.2017.01.051

upstream raw materials:

N-benzyl-N-(4-methylphenyl)amine

methyl iodide

4-tolyl iodide

benzyl-methyl-amine

Downstream raw materials:

N-benzyl-N-methyl-p-toluidine-N-oxide

N-methyl-N-nitroso-p-toluidine

N-benzyl-N-(p-tolyl)formamide

4-(N-methylacetamido)toluene

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