4-methoxy-2-[4-(trifluoromethyl)phenyl]-5-[[3-(trifluoromethyl)-1H-pyrazol-1-yl]methyl]-2H-1,2,3-triazole

Base Information

• Chemical Name: 4-methoxy-2-[4-(trifluoromethyl)phenyl]-5-[[3-(trifluoromethyl)-1H-pyrazol-1-yl]methyl]-2H-1,2,3-triazole
• CAS No.: 1606030-43-6
• Molecular Formula: C₁₅H₁₁F₆N₅O
• Molecular Weight: 391.276
• Mol file: 1606030-43-6.mol

Synonyms:4-methoxy-2-[4-(trifluoromethyl)phenyl]-5-[[3-(trifluoromethyl)-1H-pyrazol-1-yl]methyl]-2H-1,2,3-triazole

Chemical Property of 4-methoxy-2-[4-(trifluoromethyl)phenyl]-5-[[3-(trifluoromethyl)-1H-pyrazol-1-yl]methyl]-2H-1,2,3-triazole

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 4-methoxy-2-[4-(trifluoromethyl)phenyl]-5-[[3-(trifluoromethyl)-1H-pyrazol-1-yl]methyl]-2H-1,2,3-triazole

There total 5 articles about 4-methoxy-2-[4-(trifluoromethyl)phenyl]-5-[[3-(trifluoromethyl)-1H-pyrazol-1-yl]methyl]-2H-1,2,3-triazole 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:

3-(trifluoromethyl)pyrazole (20154-03-4) + 4-(bromomethyl)-5-methoxy-2-[4-(trifluoromethyl)phenyl]-2H-1,2,3-triazole (1607442-62-5) → 4-methoxy-2-[4-(trifluoromethyl)phenyl]-5-[[3-(trifluoromethyl)-1H-pyrazol-1-yl]methyl]-2H-1,2,3-triazole (1606030-43-6)

Guidance literature:

With potassium carbonate; In N,N-dimethyl-formamide; at 55 ℃; for 1.25h;

Reference yield:

4-(trifluoromethyl)phenylhydrazine (368-90-1) → 4-methoxy-2-[4-(trifluoromethyl)phenyl]-5-[[3-(trifluoromethyl)-1H-pyrazol-1-yl]methyl]-2H-1,2,3-triazole (1606030-43-6)

Guidance literature:

Multi-step reaction with 5 steps

1.1: diethyl ether / 2 h / 23 °C

1.2: 17 h / Reflux

2.1: dichloromethane / 65 h / 23 °C

3.1: sodium methylate / methanol / 6 h / 23 °C

4.1: N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile) / tetrachloromethane / 4.5 h / Reflux

5.1: potassium carbonate / N,N-dimethyl-formamide / 1.25 h / 55 °C

With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); sodium methylate; potassium carbonate; In methanol; tetrachloromethane; diethyl ether; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

4-methoxy-5-methyl-2-[4-(trifluoromethyl)phenyl]-2H-1,2,3-triazole (1607442-61-4) → 4-methoxy-2-[4-(trifluoromethyl)phenyl]-5-[[3-(trifluoromethyl)-1H-pyrazol-1-yl]methyl]-2H-1,2,3-triazole (1606030-43-6)

Guidance literature:

Multi-step reaction with 2 steps

1: N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile) / tetrachloromethane / 4.5 h / Reflux

2: potassium carbonate / N,N-dimethyl-formamide / 1.25 h / 55 °C

With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); potassium carbonate; In tetrachloromethane; N,N-dimethyl-formamide;

upstream raw materials:

4-(trifluoromethyl)phenylhydrazine

4-methyl-2-[4-(trifluoromethyl)phenyl]-2H-1,2,3-triazole 1-oxide

1-methoxy-4-methyl-2-[4-(trifluoromethyl)phenyl]-2H-1,2,3-triazolium tetrafluoroborate

4-methoxy-5-methyl-2-[4-(trifluoromethyl)phenyl]-2H-1,2,3-triazole