Benzenamine, N-dodecyl-N-phenyl-

Base Information

• Chemical Name: Benzenamine, N-dodecyl-N-phenyl-
• CAS No.: 78204-99-6
• Molecular Formula: C24H35N
• Molecular Weight: 337.549
• DSSTox Substance ID: DTXSID30400711
• Mol file: 78204-99-6.mol

Synonyms:Benzenamine, N-dodecyl-N-phenyl-;N-dodecyldiphenylamine;78204-99-6;SCHEMBL44732;DTXSID30400711

Chemical Property of Benzenamine, N-dodecyl-N-phenyl-

Chemical Property:

• XLogP3: 9.2
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 13
• Exact Mass: 337.276950121
• Heavy Atom Count: 25
• Complexity: 271

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCCCCCN(C1=CC=CC=C1)C2=CC=CC=C2

Technology Process of Benzenamine, N-dodecyl-N-phenyl-

There total 2 articles about Benzenamine, N-dodecyl-N-phenyl- 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: 59.0%

n-Dodecylamine (124-22-1) + chlorobenzene (108-90-7) → N-dodecylaniline (3007-74-7) + N-dodecyldiphenylamine (78204-99-6)

Guidance literature:

With potassium tert-butylate; In 1,4-dioxane; at 110 ℃; for 3h;

DOI:10.1016/j.jorganchem.2007.05.022

Reference yield: 58.0%

1-dodecylbromide (143-15-7) + diphenylamine (122-39-4) → N-dodecyldiphenylamine (78204-99-6)

Guidance literature:

With potassium hydroxide; tetrabutyliodide; In toluene; for 0.8h; Irradiation;

DOI:10.1016/S0040-4039(00)94235-7

Reference yield:

N-dodecyldiphenylamine (78204-99-6) + N,N-dimethyl-formamide (68-12-2,33513-42-7) → C26H35NO2

Guidance literature:

N,N-dimethyl-formamide; With trichlorophosphate; at 0 ℃;

N-dodecyldiphenylamine; at 90 ℃; for 20h;

DOI:10.1016/j.molstruc.2017.10.058

upstream raw materials:

1-dodecylbromide

diphenylamine

n-Dodecylamine

chlorobenzene

Refernces

• 1、 Li, Jingya,Cui, Mengjun,Yu, Ajuan,Wu, Yangjie. "Carbene adduct of cyclopalladated ferrocenylimine as an efficient catalyst for the amination of aryl chlorides". . p. 3732 - 3742. Retrieved 2008/02/08.