4-(4-bromo-1-(2-methyl-3-(trifluoromethyl)benzyl)-1H-benzo[d]imidazol-6-yl)morpholine

Base Information

• Chemical Name: 4-(4-bromo-1-(2-methyl-3-(trifluoromethyl)benzyl)-1H-benzo[d]imidazol-6-yl)morpholine
• CAS No.: 1443541-22-7
• Molecular Formula: C₂₀H₁₉BrF₃N₃O
• Molecular Weight: 454.29
• Mol file: 1443541-22-7.mol

Synonyms:4-(4-bromo-1-(2-methyl-3-(trifluoromethyl)benzyl)-1H-benzo[d]imidazol-6-yl)morpholine

Chemical Property of 4-(4-bromo-1-(2-methyl-3-(trifluoromethyl)benzyl)-1H-benzo[d]imidazol-6-yl)morpholine

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 4-(4-bromo-1-(2-methyl-3-(trifluoromethyl)benzyl)-1H-benzo[d]imidazol-6-yl)morpholine

There total 5 articles about 4-(4-bromo-1-(2-methyl-3-(trifluoromethyl)benzyl)-1H-benzo[d]imidazol-6-yl)morpholine 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: 18.84%

1,1'-oxybis(2-bromo-ethane) (5414-19-7) + 4-bromo-1-(2-methyl-3-(trifluoromethyl)benzyl)-1H-benzo[d]imidazol-6-amine (1443541-21-6) → 4-(4-bromo-1-(2-methyl-3-(trifluoromethyl)benzyl)-1H-benzo[d]imidazol-6-yl)morpholine (1443541-22-7)

Guidance literature:

With tetra-(n-butyl)ammonium iodide; sodium hydroxide; In water; at 110 ℃; for 2h;

Reference yield:

4-bromo-6-nitro-1H-benzo[d]imidazole (206759-50-4) → 4-(4-bromo-1-(2-methyl-3-(trifluoromethyl)benzyl)-1H-benzo[d]imidazol-6-yl)morpholine (1443541-22-7)

Guidance literature:

Multi-step reaction with 3 steps

1: potassium carbonate / N,N-dimethyl-formamide / 1 h / 60 °C

2: hydrogenchloride; tin(II) chloride dihdyrate / water; methanol / 1 h / 80 °C

3: sodium hydroxide; tetra-(n-butyl)ammonium iodide / water / 2 h / 110 °C

With hydrogenchloride; tin(II) chloride dihdyrate; tetra-(n-butyl)ammonium iodide; potassium carbonate; sodium hydroxide; In methanol; water; N,N-dimethyl-formamide;

Reference yield:

4-bromo-1-(2-methyl-3-(trifluoromethyl)benzyl)-6-nitro-1H-benzo[d]imidazole (1443541-20-5) → 4-(4-bromo-1-(2-methyl-3-(trifluoromethyl)benzyl)-1H-benzo[d]imidazol-6-yl)morpholine (1443541-22-7)

Guidance literature:

Multi-step reaction with 2 steps

1: hydrogenchloride; tin(II) chloride dihdyrate / water; methanol / 1 h / 80 °C

2: sodium hydroxide; tetra-(n-butyl)ammonium iodide / water / 2 h / 110 °C

With hydrogenchloride; tin(II) chloride dihdyrate; tetra-(n-butyl)ammonium iodide; sodium hydroxide; In methanol; water;

upstream raw materials:

4-bromo-6-nitro-1H-benzo[d]imidazole

4-bromo-1-(2-methyl-3-(trifluoromethyl)benzyl)-6-nitro-1H-benzo[d]imidazole

1,1'-oxybis(2-bromo-ethane)

4-bromo-1-(2-methyl-3-(trifluoromethyl)benzyl)-1H-benzo[d]imidazol-6-amine