(2-Nitrophenyl)(2-phenylethyl)amine

Base Information

• Chemical Name: (2-Nitrophenyl)(2-phenylethyl)amine
• CAS No.: 100870-32-4
• Molecular Formula: C14H14N2O2
• Molecular Weight: 242.277
• DSSTox Substance ID: DTXSID00387823
• Wikidata: Q82182334
• Mol file: 100870-32-4.mol

Synonyms:(2-nitrophenyl)(2-phenylethyl)amine;100870-32-4;2-nitro-N-(2-phenylethyl)aniline;2-nitro-N-phenethylaniline;N-phenethyl-2-nitroaniline;N-Phenylethyl-2-nitroaniline;Oprea1_161743;SCHEMBL103245;2-nitro-N-phenethylbenzenamine;DTXSID00387823;ROBBUBPDMDQMGG-UHFFFAOYSA-N;n-(2-phenylethyl)-2-nitroaniline;MFCD01907051;STK149444;AKOS001057093;SB80836;LS-08396;CS-0269938;SR-01000247624;SR-01000247624-1;Z31198320;F1244-0037

Chemical Property of (2-Nitrophenyl)(2-phenylethyl)amine

Chemical Property:

• PSA: 57.85000
• LogP: 3.84560
• XLogP3: 4.1
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 4
• Exact Mass: 242.105527694
• Heavy Atom Count: 18
• Complexity: 259

Purity/Quality:

97% ^*data from raw suppliers

2-Nitro-N-phenethylaniline 97% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC=C(C=C1)CCNC2=CC=CC=C2[N+](=O)[O-]

Technology Process of (2-Nitrophenyl)(2-phenylethyl)amine

There total 6 articles about (2-Nitrophenyl)(2-phenylethyl)amine 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: 97.0%

N,N-diispropylethylamine + phenethylamine (64-04-0) + 2-Chloronitrobenzene (88-73-3) → N-(2-Phenylethyl)-2-nitroaniline (100870-32-4)

Guidance literature:

In ethyl acetate; 1,2-dichloro-ethane;

Reference yield: 94.0%

phenethylamine (64-04-0) + ortho-nitrofluorobenzene (1493-27-2,127723-77-7) → N-(2-Phenylethyl)-2-nitroaniline (100870-32-4)

Guidance literature:

With triethylamine; In neat (no solvent); at 140 ℃; for 9h;

DOI:10.1016/j.tetlet.2020.151599

Reference yield: 63.0%

phenethylamine (64-04-0) + potassium o-nitrobenzoate (15163-59-4) → N-(2-Phenylethyl)-2-nitroaniline (100870-32-4)

Guidance literature:

With copper(l) iodide; 1,10-Phenanthroline; tetraammine palladium hydrogen carbonate; 4-methylmorpholine N-oxide; In N,N-dimethyl acetamide; at 145 ℃; for 16h; Reagent/catalyst; Concentration; Sealed tube;

DOI:10.1002/anie.201812068

upstream raw materials:

phenethylamine

2-Chloronitrobenzene

ortho-nitrofluorobenzene

1-phenyl-2-bromoethane

Downstream raw materials:

N-(2-phenylethyl)-2-aminoaniline