{1-methyl-6-[3-(trifluoromethyl)phenoxy]-1H-benzimidazol-2-yl}methanol

Base Information

Chemical Name:{1-methyl-6-[3-(trifluoromethyl)phenoxy]-1H-benzimidazol-2-yl}methanol
CAS No.:1072003-26-9
Molecular Formula:C₁₆H₁₃F₃N₂O₂
Molecular Weight:322.287
Hs Code.:

Synonyms:{1-methyl-6-[3-(trifluoromethyl)phenoxy]-1H-benzimidazol-2-yl}methanol

Suppliers and Price of {1-methyl-6-[3-(trifluoromethyl)phenoxy]-1H-benzimidazol-2-yl}methanol

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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 {1-methyl-6-[3-(trifluoromethyl)phenoxy]-1H-benzimidazol-2-yl}methanol

Chemical Property:

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Technology Process of {1-methyl-6-[3-(trifluoromethyl)phenoxy]-1H-benzimidazol-2-yl}methanol

There total 3 articles about {1-methyl-6-[3-(trifluoromethyl)phenoxy]-1H-benzimidazol-2-yl}methanol 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: 57.0%

: 1072003-26-9
{1-methyl-6-[3-(trifluoromethyl)phenoxy]-1H-benzimidazol-2-yl}methanol

Guidance literature:

Reference yield:

: 79-14-1
glycolic Acid

: 1072003-25-8
tert-butyl {2-amino-5-[3-(trifluoromethyl)phenoxy]phenyl}methylcarbamate

: 1072003-26-9
{1-methyl-6-[3-(trifluoromethyl)phenoxy]-1H-benzimidazol-2-yl}methanol

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; water; for 2h; Reflux;
DOI:10.1016/j.bmc.2018.09.006

Reference yield:

: 299176-17-3
N-(2-nitro-5-chlorophenyl)-N-methylcarbamic acid t-butyl ester

: 1072003-26-9
{1-methyl-6-[3-(trifluoromethyl)phenoxy]-1H-benzimidazol-2-yl}methanol

Guidance literature:: Multi-step reaction with 3 steps

1: sodium hydride / N,N-dimethyl-formamide / 10 h / 80 °C / Inert atmosphere

2: iron; ammonium chloride / ethanol; water / 5 h / Reflux

3: hydrogenchloride / 1,4-dioxane; water / 2 h / Reflux

With hydrogenchloride; iron; sodium hydride; ammonium chloride; In 1,4-dioxane; ethanol; water; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2018.09.006