4-[3-(2-bromobenzyl)-4,4-dimethyl-2,5-dioxoimidazolidin-1-yl]-2-trifluoromethylbenzonitrile

Base Information

Chemical Name:4-[3-(2-bromobenzyl)-4,4-dimethyl-2,5-dioxoimidazolidin-1-yl]-2-trifluoromethylbenzonitrile
CAS No.:1006898-69-6
Molecular Formula:C₂₀H₁₅BrF₃N₃O₂
Molecular Weight:466.257
Hs Code.:

Synonyms:4-[3-(2-bromobenzyl)-4,4-dimethyl-2,5-dioxoimidazolidin-1-yl]-2-trifluoromethylbenzonitrile

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Chemical Property of 4-[3-(2-bromobenzyl)-4,4-dimethyl-2,5-dioxoimidazolidin-1-yl]-2-trifluoromethylbenzonitrile

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Technology Process of 4-[3-(2-bromobenzyl)-4,4-dimethyl-2,5-dioxoimidazolidin-1-yl]-2-trifluoromethylbenzonitrile

There total 5 articles about 4-[3-(2-bromobenzyl)-4,4-dimethyl-2,5-dioxoimidazolidin-1-yl]-2-trifluoromethylbenzonitrile 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: 86.0%

: 143782-20-1
4-(4,4-dimethyl-2,5-dioxoimidazolidin-1-yl)-2-(trifluoromethyl)benzonitrile

: 3433-80-5
1-Bromo-2-bromomethyl-benzene

: 1006898-69-6
4-[3-(2-bromobenzyl)-4,4-dimethyl-2,5-dioxoimidazolidin-1-yl]-2-trifluoromethylbenzonitrile

Guidance literature:: With potassium carbonate; In acetonitrile; at 20 ℃; for 5h;

Reference yield:

: 654-70-6
4-amino-2-trifluoromethylbenzonitrile

: 1006898-69-6
4-[3-(2-bromobenzyl)-4,4-dimethyl-2,5-dioxoimidazolidin-1-yl]-2-trifluoromethylbenzonitrile

Guidance literature:: Multi-step reaction with 4 steps

1: acetonitrile / 70 °C

2: triethylamine / acetonitrile / 0.75 h / 20 °C

3: hydrogenchloride / acetonitrile; water / 1 h / 70 °C

4: potassium carbonate / acetonitrile / 5 h / 20 °C

With hydrogenchloride; potassium carbonate; triethylamine; In water; acetonitrile;

Reference yield:

: 143782-18-7
4-isocyanato-2-(trifluoromethyl)benzonitrile

: 1006898-69-6
4-[3-(2-bromobenzyl)-4,4-dimethyl-2,5-dioxoimidazolidin-1-yl]-2-trifluoromethylbenzonitrile

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine / acetonitrile / 0.75 h / 20 °C

2: hydrogenchloride / acetonitrile; water / 1 h / 70 °C

3: potassium carbonate / acetonitrile / 5 h / 20 °C

With hydrogenchloride; potassium carbonate; triethylamine; In water; acetonitrile;