N-Butyl-N-phenylbenzenemethanamine

Base Information

• Chemical Name: N-Butyl-N-phenylbenzenemethanamine
• CAS No.: 187101-95-7
• Molecular Formula: C₁₇H₂₁N
• Molecular Weight: 239.36
• DSSTox Substance ID: DTXSID301295508
• Nikkaji Number: J2.442.840K
• Mol file: 187101-95-7.mol

Synonyms:SCHEMBL627791;N-Butyl-N-phenylbenzenemethanamine;DTXSID301295508;187101-95-7

Chemical Property of N-Butyl-N-phenylbenzenemethanamine

Chemical Property:

• XLogP3: 5.5
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 6
• Exact Mass: 239.167399674
• Heavy Atom Count: 18
• Complexity: 202

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: CCCCN(CC1=CC=CC=C1)C2=CC=CC=C2

Technology Process of N-Butyl-N-phenylbenzenemethanamine

There total 11 articles about N-Butyl-N-phenylbenzenemethanamine 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: 93.0%

N-(n-butyl)aniline (1126-78-9) + benzyl bromide (100-39-0) → benzyl(butyl)phenylamine (187101-95-7)

Guidance literature:

With sodium dodecyl-sulfate; sodium hydrogencarbonate; In water; at 80 ℃; for 1h;

DOI:10.1002/ejoc.200600937

Reference yield: 83.0%

aniline (62-53-3) + benzyl alcohol (100-51-6,185532-71-2) + butan-1-ol (71-36-3) → benzyl(butyl)phenylamine (187101-95-7)

Guidance literature:

With Cu₂Al₃Ox-HT; In toluene; at 160 ℃; for 24h; Inert atmosphere; Sealed tube;

DOI:10.1039/c5cc02205c

Reference yield: 53.0%

2-(benzyl(Butyl)amino)benzaldehyde → benzyl(butyl)phenylamine (187101-95-7)

Guidance literature:

With 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone; at 20 ℃; for 6h; Irradiation; Inert atmosphere; Green chemistry;

DOI:10.1039/d0gc01256d

upstream raw materials:

1-iodo-butane

N-Benzylaniline

N-(n-butyl)aniline

benzyl chloride

Downstream raw materials:

N-benzyl-N-butyl-p-phenylenediamine