(4-FLUORO-BENZYLIDENE)-[2-METHYL-5-(4-TRIFLUOROMETHYL-PHENYL)-2H-PYRAZOL-3-YL]-amine

Base Information

Chemical Name:(4-FLUORO-BENZYLIDENE)-[2-METHYL-5-(4-TRIFLUOROMETHYL-PHENYL)-2H-PYRAZOL-3-YL]-amine
CAS No.:639784-35-3
Molecular Formula:C₁₈H₁₃F₄N₃
Molecular Weight:347.315
Hs Code.:

Synonyms:(4-FLUORO-BENZYLIDENE)-[2-METHYL-5-(4-TRIFLUOROMETHYL-PHENYL)-2H-PYRAZOL-3-YL]-amine

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Chemical Property of (4-FLUORO-BENZYLIDENE)-[2-METHYL-5-(4-TRIFLUOROMETHYL-PHENYL)-2H-PYRAZOL-3-YL]-amine

Chemical Property:

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Technology Process of (4-FLUORO-BENZYLIDENE)-[2-METHYL-5-(4-TRIFLUOROMETHYL-PHENYL)-2H-PYRAZOL-3-YL]-amine

There total 4 articles about (4-FLUORO-BENZYLIDENE)-[2-METHYL-5-(4-TRIFLUOROMETHYL-PHENYL)-2H-PYRAZOL-3-YL]-amine 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:

: 2967-66-0
methyl 4-(trifluoromethyl)benzoate

: 639784-35-3
(4-FLUORO-BENZYLIDENE)-[2-METHYL-5-(4-TRIFLUOROMETHYL-PHENYL)-2H-PYRAZOL-3-YL]-amine

Guidance literature:: Multi-step reaction with 3 steps

1: acetonitrile / chlorobenzene / 30 h

2: methylhydrazine / ethanol / 3 h

3: 3-thiophene carboxaldehyde / ethanol / 12 h

With 3-thiophene carboxaldehyde; methylhydrazine; acetonitrile; In ethanol; chlorobenzene;

Reference yield:

: 639784-30-8
1-methyl-3-(4-(trifluoromethyl)phenyl)-1H-pyrazol-5-amine

: 639784-35-3
(4-FLUORO-BENZYLIDENE)-[2-METHYL-5-(4-TRIFLUOROMETHYL-PHENYL)-2H-PYRAZOL-3-YL]-amine

Guidance literature:: With 3-thiophene carboxaldehyde; In ethanol; for 12h;

Reference yield:

: 455-24-3
4-trifluoromethylbenzoic acid

: 639784-35-3
(4-FLUORO-BENZYLIDENE)-[2-METHYL-5-(4-TRIFLUOROMETHYL-PHENYL)-2H-PYRAZOL-3-YL]-amine

Guidance literature:: Multi-step reaction with 4 steps

1.1: thionyl chloride / toluene / 3 h

1.2: 15 h / 30 - 60 °C

2.1: acetonitrile / chlorobenzene / 30 h

3.1: methylhydrazine / ethanol / 3 h

4.1: 3-thiophene carboxaldehyde / ethanol / 12 h

With 3-thiophene carboxaldehyde; thionyl chloride; methylhydrazine; acetonitrile; In ethanol; chlorobenzene; toluene;