4-[2,5-dioxo-4-[(2-propenyloxy)methyl]-3-(1-methylethyl)-4-phenylimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile

Base Information

• Chemical Name: 4-[2,5-dioxo-4-[(2-propenyloxy)methyl]-3-(1-methylethyl)-4-phenylimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile
• CAS No.: 1215086-16-0
• Molecular Formula: C₂₄H₂₂F₃N₃O₃
• Molecular Weight: 457.452

Synonyms:4-[2,5-dioxo-4-[(2-propenyloxy)methyl]-3-(1-methylethyl)-4-phenylimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile

Chemical Property of 4-[2,5-dioxo-4-[(2-propenyloxy)methyl]-3-(1-methylethyl)-4-phenylimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile

Chemical Property:

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Technology Process of 4-[2,5-dioxo-4-[(2-propenyloxy)methyl]-3-(1-methylethyl)-4-phenylimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile

There total 4 articles about 4-[2,5-dioxo-4-[(2-propenyloxy)methyl]-3-(1-methylethyl)-4-phenylimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile 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:

2-iodo-propane (75-30-9) + 4-[2,5-dioxo-4-phenyl-4-[(2-propenyloxy)methyl]imidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile (1215085-66-7) → 4-[2,5-dioxo-4-[(2-propenyloxy)methyl]-3-(1-methylethyl)-4-phenylimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile (1215086-16-0)

Guidance literature:

With potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 4h; Inert atmosphere;

DOI:10.1021/jm300281x

Reference yield:

4-bromo-2-(trifluoromethyl)benzonitrile (191165-13-6) → 4-[2,5-dioxo-4-[(2-propenyloxy)methyl]-3-(1-methylethyl)-4-phenylimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile (1215086-16-0)

Guidance literature:

Multi-step reaction with 2 steps

1: copper(I) oxide / N,N-dimethyl acetamide / 3 h / 160 °C / Inert atmosphere

2: potassium carbonate / N,N-dimethyl-formamide / 4 h / 20 °C / Inert atmosphere

With copper(I) oxide; potassium carbonate; In N,N-dimethyl acetamide; N,N-dimethyl-formamide;

DOI:10.1021/jm300281x

Reference yield:

5-phenyl-5-(2-propenyloxy)methylimidazolidine-2,4-dione (1215085-65-6) → 4-[2,5-dioxo-4-[(2-propenyloxy)methyl]-3-(1-methylethyl)-4-phenylimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile (1215086-16-0)

Guidance literature:

Multi-step reaction with 2 steps

1: copper(I) oxide / N,N-dimethyl acetamide / 3 h / 160 °C / Inert atmosphere

2: potassium carbonate / N,N-dimethyl-formamide / 4 h / 20 °C / Inert atmosphere

With copper(I) oxide; potassium carbonate; In N,N-dimethyl acetamide; N,N-dimethyl-formamide;

DOI:10.1021/jm300281x

upstream raw materials:

4-bromo-2-(trifluoromethyl)benzonitrile

2-iodo-propane

4-[2,5-dioxo-4-phenyl-4-[(2-propenyloxy)methyl]imidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile

5-phenyl-5-(2-propenyloxy)methylimidazolidine-2,4-dione

Downstream raw materials:

4-[2,5-dioxo-4-hydroxymethyl-3-(1-methylethyl)-4-phenylimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile

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