4-[4-allyloxymethyl-4-(2-chlorophenyl)-2,5-dioxoimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile

Base Information

Chemical Name:4-[4-allyloxymethyl-4-(2-chlorophenyl)-2,5-dioxoimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile
CAS No.:1401225-65-7
Molecular Formula:C₂₁H₁₅ClF₃N₃O₃
Molecular Weight:449.817
Hs Code.:

Synonyms:4-[4-allyloxymethyl-4-(2-chlorophenyl)-2,5-dioxoimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile

Suppliers and Price of 4-[4-allyloxymethyl-4-(2-chlorophenyl)-2,5-dioxoimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of 4-[4-allyloxymethyl-4-(2-chlorophenyl)-2,5-dioxoimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 4-[4-allyloxymethyl-4-(2-chlorophenyl)-2,5-dioxoimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile

There total 1 articles about 4-[4-allyloxymethyl-4-(2-chlorophenyl)-2,5-dioxoimidazolidin-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:

: 191165-13-6
4-bromo-2-(trifluoromethyl)benzonitrile

: 1401225-49-7
5-allyloxymethyl-5-(2-chlorophenyl)imidazolidine-2,4-dione

: 1401225-65-7
4-[4-allyloxymethyl-4-(2-chlorophenyl)-2,5-dioxoimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile

Guidance literature:: With copper(I) oxide; In N,N-dimethyl acetamide; at 160 ℃; for 4h; Inert atmosphere;
DOI:10.1021/jm300281x

Reference yield:

: 1401225-65-7
4-[4-allyloxymethyl-4-(2-chlorophenyl)-2,5-dioxoimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile

: 74-88-4
methyl iodide

: 1215086-28-4
4-[4-allyloxymethyl-4-(2-chlorophenyl)-3-methyl-2,5-dioxoimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 6h; Inert atmosphere;
DOI:10.1021/jm300281x

Reference yield:

: 1401225-65-7
4-[4-allyloxymethyl-4-(2-chlorophenyl)-2,5-dioxoimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile

: 1215086-27-3
4-[4-(2-chlorophenyl)-2,5-dioxo-4-hydroxymethyl-3-methylimidazolidin-1-yl]-2-(trifluoromethyl)benzonitrile

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / N,N-dimethyl-formamide / 6 h / 20 °C / Inert atmosphere

2: boron dimethyl-trifluoro sulphide / dichloromethane / 6 h / 20 °C / Inert atmosphere

With boron dimethyl-trifluoro sulphide; potassium carbonate; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm300281x