3-<<2-(5-methyl-4-phenyl-1H-imidazol-1-yl)ethoxy>methyl>-2-nitrotoluene

Base Information

Chemical Name:3-<<2-(5-methyl-4-phenyl-1H-imidazol-1-yl)ethoxy>methyl>-2-nitrotoluene
CAS No.:148726-35-6
Molecular Formula:C₂₀H₂₁N₃O₃
Molecular Weight:351.405
Hs Code.:

Synonyms:3-<<2-(5-methyl-4-phenyl-1H-imidazol-1-yl)ethoxy>methyl>-2-nitrotoluene

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

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Chemical Property of 3-<<2-(5-methyl-4-phenyl-1H-imidazol-1-yl)ethoxy>methyl>-2-nitrotoluene

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Technology Process of 3-<<2-(5-methyl-4-phenyl-1H-imidazol-1-yl)ethoxy>methyl>-2-nitrotoluene

There total 1 articles about 3-<<2-(5-methyl-4-phenyl-1H-imidazol-1-yl)ethoxy>methyl>-2-nitrotoluene 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: 54.0%

: 55324-02-2
1-(bromomethyl)-3-methyl-2-nitrobenzene

: 1-(2-hydroxyethyl)-5-methyl-4-phenylimidazole

: 148726-35-6
3-<<2-(5-methyl-4-phenyl-1H-imidazol-1-yl)ethoxy>methyl>-2-nitrotoluene

Guidance literature:: With sodium hydride; In N,N-dimethyl-formamide; for 0.166667h; Ambient temperature;
DOI:10.1021/jm00063a014

Reference yield: 45.0%

: 148726-35-6
3-<<2-(5-methyl-4-phenyl-1H-imidazol-1-yl)ethoxy>methyl>-2-nitrotoluene

: 148726-70-9
2-methyl-6-<<2-(5-methyl-4-phenyl-1H-imidazol-1-yl)ethoxy>methyl>aniline

Guidance literature:: With acetic acid; zinc; for 0.5h; Ambient temperature;
DOI:10.1021/jm00063a014

Reference yield:

: 148726-35-6
3-<<2-(5-methyl-4-phenyl-1H-imidazol-1-yl)ethoxy>methyl>-2-nitrotoluene

: N-[2-{2-(5-methyl-4-phenyl-1H-imidazol-1-yl)}ethyloxy-methyl-6-methyl]phenyl-N'-pentylurea

Guidance literature:: Multi-step reaction with 2 steps

1: 45 percent / zinc, AcOH / 0.5 h / Ambient temperature

2: 60 percent / benzene / 1.5 h / Heating

With acetic acid; zinc; In benzene;
DOI:10.1021/jm00063a014