N-[5-(4-Chloro-1-methyl-5-trifluoromethyl-1H-pyrazol-3-yloxy)-2-trifluoromethyl-phenyl]-N-methyl-acetamide

Base Information

Chemical Name:N-[5-(4-Chloro-1-methyl-5-trifluoromethyl-1H-pyrazol-3-yloxy)-2-trifluoromethyl-phenyl]-N-methyl-acetamide
CAS No.:182289-24-3
Molecular Formula:C₁₅H₁₂ClF₆N₃O₂
Molecular Weight:415.723
Hs Code.:

Synonyms:N-[5-(4-Chloro-1-methyl-5-trifluoromethyl-1H-pyrazol-3-yloxy)-2-trifluoromethyl-phenyl]-N-methyl-acetamide

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Chemical Property of N-[5-(4-Chloro-1-methyl-5-trifluoromethyl-1H-pyrazol-3-yloxy)-2-trifluoromethyl-phenyl]-N-methyl-acetamide

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Technology Process of N-[5-(4-Chloro-1-methyl-5-trifluoromethyl-1H-pyrazol-3-yloxy)-2-trifluoromethyl-phenyl]-N-methyl-acetamide

There total 6 articles about N-[5-(4-Chloro-1-methyl-5-trifluoromethyl-1H-pyrazol-3-yloxy)-2-trifluoromethyl-phenyl]-N-methyl-acetamide 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: 79.0%

: 182288-81-9
N-[5-(4-Chloro-1-methyl-5-trifluoromethyl-1H-pyrazol-3-yloxy)-2-trifluoromethyl-phenyl]-acetamide

: 182289-24-3
N-[5-(4-Chloro-1-methyl-5-trifluoromethyl-1H-pyrazol-3-yloxy)-2-trifluoromethyl-phenyl]-N-methyl-acetamide

Guidance literature:: With potassium hydroxide; In dichloromethane;
DOI:10.1021/jf9601978

Reference yield:

: 349-27-9
N-(2-fluoro-5-(trifluoromethyl)phenyl)acetamide

: 182289-24-3
N-[5-(4-Chloro-1-methyl-5-trifluoromethyl-1H-pyrazol-3-yloxy)-2-trifluoromethyl-phenyl]-N-methyl-acetamide

Guidance literature:: Multi-step reaction with 6 steps

1: 1.) conc. H₂SO₄, HNO₃, 2.) 12 N aq. HCl, 3.) t-BuONO

2: 73 percent / K₂CO₃ / dimethylsulfoxide / Heating

3: 63 percent / dichlorodimethylhydantoin / acetonitrile

4: 97 percent / aq. AcOH, Fe / 0.5 h / 80 °C

5: 95 percent / 3 h / Heating

6: 79 percent / KOH / CH₂Cl₂

With hydrogenchloride; potassium hydroxide; tert.-butylnitrite; 1,3-dichloro-5,5-dimethylhydantoin; sulfuric acid; nitric acid; iron; potassium carbonate; acetic acid; In dichloromethane; dimethyl sulfoxide; acetonitrile;
DOI:10.1021/jf9601978

Reference yield:

: 182289-81-2
4-fluoro-3-nitrobenzotrifluoride

: 182289-24-3
N-[5-(4-Chloro-1-methyl-5-trifluoromethyl-1H-pyrazol-3-yloxy)-2-trifluoromethyl-phenyl]-N-methyl-acetamide

Guidance literature:: Multi-step reaction with 5 steps

1: 73 percent / K₂CO₃ / dimethylsulfoxide / Heating

2: 63 percent / dichlorodimethylhydantoin / acetonitrile

3: 97 percent / aq. AcOH, Fe / 0.5 h / 80 °C

4: 95 percent / 3 h / Heating

5: 79 percent / KOH / CH₂Cl₂

With potassium hydroxide; 1,3-dichloro-5,5-dimethylhydantoin; iron; potassium carbonate; acetic acid; In dichloromethane; dimethyl sulfoxide; acetonitrile;
DOI:10.1021/jf9601978