1-(2-((4-(tert-butyl)benzyl)oxy)-2-(2,4-dichlorophenyl)ethyl)-1H-imidazole

Base Information

Chemical Name:1-(2-((4-(tert-butyl)benzyl)oxy)-2-(2,4-dichlorophenyl)ethyl)-1H-imidazole
CAS No.:47545-72-2
Molecular Formula:C₂₂H₂₄Cl₂N₂O
Molecular Weight:403.351
Hs Code.:

Synonyms:1-(2-((4-(tert-butyl)benzyl)oxy)-2-(2,4-dichlorophenyl)ethyl)-1H-imidazole

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Chemical Property of 1-(2-((4-(tert-butyl)benzyl)oxy)-2-(2,4-dichlorophenyl)ethyl)-1H-imidazole

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Technology Process of 1-(2-((4-(tert-butyl)benzyl)oxy)-2-(2,4-dichlorophenyl)ethyl)-1H-imidazole

There total 6 articles about 1-(2-((4-(tert-butyl)benzyl)oxy)-2-(2,4-dichlorophenyl)ethyl)-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: 57.1%

: 24155-42-8
1-(2,4-dichlorophenyl)-2-(1H-imidazol-1-yl)ethan-1-ol

: 47545-72-2
1-(2-((4-(tert-butyl)benzyl)oxy)-2-(2,4-dichlorophenyl)ethyl)-1H-imidazole

Guidance literature:: 1-(2,4-dichlorophenyl)-2-(1H-imidazol-1-yl)ethan-1-ol; With sodium hydride; In N,N-dimethyl-formamide; at -5 - 20 ℃; for 1.5h; Inert atmosphere;

tert-butylbenzyl halide; In N,N-dimethyl-formamide; at 0 - 20 ℃; for 1h; Inert atmosphere;
DOI:10.1016/j.bmc.2018.02.014

Reference yield: 35.0%

: 18880-00-7
1-(bromomethyl)-4-(1,1-dimethylethyl)benzene

: 24155-42-8
1-(2,4-dichlorophenyl)-2-(1H-imidazol-1-yl)ethan-1-ol

: 47545-72-2
1-(2-((4-(tert-butyl)benzyl)oxy)-2-(2,4-dichlorophenyl)ethyl)-1H-imidazole

Guidance literature:: With N,N,N,N,N,N-hexamethylphosphoric triamide; tetra-(n-butyl)ammonium iodide; sodium hydride; at 0 ℃;

Reference yield:

: 2631-72-3
2,4-dichlorophenacyl bromide

: 47545-72-2
1-(2-((4-(tert-butyl)benzyl)oxy)-2-(2,4-dichlorophenyl)ethyl)-1H-imidazole

Guidance literature:: Multi-step reaction with 3 steps

1: CHCl₃ / 0 °C

2: sodium borohydride / ethanol / 4 h / Heating

3: 35 percent / sodium hydride in oil; HMPA; tetrabutylammonium iodide / 0 °C

With N,N,N,N,N,N-hexamethylphosphoric triamide; sodium tetrahydroborate; tetra-(n-butyl)ammonium iodide; sodium hydride; In ethanol; chloroform;