2-[4-(5-Bromo-2-benzofuranyl)phenyl]-4,5-dihydro-1H-imidazole

Base Information

Chemical Name:2-[4-(5-Bromo-2-benzofuranyl)phenyl]-4,5-dihydro-1H-imidazole
CAS No.:84102-60-3
Molecular Formula:C₁₇H₁₃BrN₂O
Molecular Weight:341.207
Hs Code.:
DSSTox Substance ID:DTXSID401181916

Synonyms:84102-60-3;DTXSID401181916;2-[4-(5-Bromo-2-benzofuranyl)phenyl]-4,5-dihydro-1H-imidazole

Suppliers and Price of 2-[4-(5-Bromo-2-benzofuranyl)phenyl]-4,5-dihydro-1H-imidazole

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 2-[4-(5-Bromo-2-benzofuranyl)phenyl]-4,5-dihydro-1H-imidazole

Chemical Property:

XLogP3:3.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:340.02113
Heavy Atom Count:21
Complexity:406

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1CN=C(N1)C2=CC=C(C=C2)C3=CC4=C(O3)C=CC(=C4)Br

Technology Process of 2-[4-(5-Bromo-2-benzofuranyl)phenyl]-4,5-dihydro-1H-imidazole

There total 4 articles about 2-[4-(5-Bromo-2-benzofuranyl)phenyl]-4,5-dihydro-1H-imidazole 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: 94.0%

: C₁₇H₁₄BrNO₂

: 107-15-3,85404-18-8
ethylenediamine

: 84102-60-3
5-Brom-2<4-(2-imidazolin-2-yl)phenyl>-1-benzofuran

Guidance literature:: In ethanol; at 20 ℃; Reflux;
DOI:10.1021/jm800918v

Reference yield:

: 84102-42-1
4-<(4-Brom-2-formylphenoxy)methyl>benzonitril

: 84102-60-3
5-Brom-2<4-(2-imidazolin-2-yl)phenyl>-1-benzofuran

Guidance literature:: Multi-step reaction with 2 steps

1: 96 percent / KOH / dimethylformamide / 2 h

2: 95 percent

With potassium hydroxide; In N,N-dimethyl-formamide;

Reference yield:

: 874-86-2
4-cyanobenzyl chloride

: 84102-60-3
5-Brom-2<4-(2-imidazolin-2-yl)phenyl>-1-benzofuran

Guidance literature:: Multi-step reaction with 3 steps

1: 1) C₂H₅ONa; 2) KI / 1) ethanol, 30 min, 80 deg C, DMF; 2) DMF, 2 h, reflux

2: 96 percent / KOH / dimethylformamide / 2 h

3: 95 percent

With potassium hydroxide; sodium ethanolate; potassium iodide; In N,N-dimethyl-formamide;