(Z)-2-((5-oxo-4-(4-(trifluoromethyl)phenyl)-4,5-dihydro-1H-tetrazol-1-yl)methyl)-3-p-tolylacrylonitrile

Base Information

• Chemical Name: (Z)-2-((5-oxo-4-(4-(trifluoromethyl)phenyl)-4,5-dihydro-1H-tetrazol-1-yl)methyl)-3-p-tolylacrylonitrile
• CAS No.: 1415645-85-0
• Molecular Formula: C₁₉H₁₄F₃N₅O
• Molecular Weight: 385.348

Synonyms:(Z)-2-((5-oxo-4-(4-(trifluoromethyl)phenyl)-4,5-dihydro-1H-tetrazol-1-yl)methyl)-3-p-tolylacrylonitrile

Chemical Property of (Z)-2-((5-oxo-4-(4-(trifluoromethyl)phenyl)-4,5-dihydro-1H-tetrazol-1-yl)methyl)-3-p-tolylacrylonitrile

Chemical Property:

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Technology Process of (Z)-2-((5-oxo-4-(4-(trifluoromethyl)phenyl)-4,5-dihydro-1H-tetrazol-1-yl)methyl)-3-p-tolylacrylonitrile

There total 4 articles about (Z)-2-((5-oxo-4-(4-(trifluoromethyl)phenyl)-4,5-dihydro-1H-tetrazol-1-yl)methyl)-3-p-tolylacrylonitrile 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: 92.0%

1-(4-trifluoromethylphenyl)-1,4-dihydrotetrazol-5-one (155431-49-5) + (2E) 2-bromomethyl-3-(4-methylphenyl)prop-2-enenitrile → (Z)-2-((5-oxo-4-(4-(trifluoromethyl)phenyl)-4,5-dihydro-1H-tetrazol-1-yl)methyl)-3-p-tolylacrylonitrile (1415645-85-0)

Guidance literature:

With potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 1h;

DOI:10.1007/s00044-012-0331-4

Reference yield:

2-(hydroxy(p-tolyl)methyl)acrylonitrile (22141-39-5) → (Z)-2-((5-oxo-4-(4-(trifluoromethyl)phenyl)-4,5-dihydro-1H-tetrazol-1-yl)methyl)-3-p-tolylacrylonitrile (1415645-85-0)

Guidance literature:

Multi-step reaction with 2 steps

1: hydrogen bromide; sulfuric acid / dichloromethane / 0 - 20 °C

2: potassium carbonate / N,N-dimethyl-formamide / 1 h / 20 °C

With sulfuric acid; hydrogen bromide; potassium carbonate; In dichloromethane; N,N-dimethyl-formamide;

DOI:10.1007/s00044-012-0331-4

Reference yield:

p-trifluoromethyl-phenylisocyanate (1548-13-6) → (Z)-2-((5-oxo-4-(4-(trifluoromethyl)phenyl)-4,5-dihydro-1H-tetrazol-1-yl)methyl)-3-p-tolylacrylonitrile (1415645-85-0)

Guidance literature:

Multi-step reaction with 2 steps

1: trimethylsilylazide / benzene / 24 h / 50 - 60 °C / Inert atmosphere

2: potassium carbonate / N,N-dimethyl-formamide / 1 h / 20 °C

With trimethylsilylazide; potassium carbonate; In N,N-dimethyl-formamide; benzene;

DOI:10.1007/s00044-012-0331-4

upstream raw materials:

2-(hydroxy(p-tolyl)methyl)acrylonitrile

1-(4-trifluoromethylphenyl)-1,4-dihydrotetrazol-5-one

p-trifluoromethyl-phenylisocyanate

4-methyl-benzaldehyde

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