1-(4-Chloro-phenyl)-3-[3-(4-chloro-phenyl)-4-hydroxy-5,5-dimethyl-2-oxo-imidazolidin-1-yl]-urea

Base Information

Chemical Name:1-(4-Chloro-phenyl)-3-[3-(4-chloro-phenyl)-4-hydroxy-5,5-dimethyl-2-oxo-imidazolidin-1-yl]-urea
CAS No.:85601-71-4
Molecular Formula:C₁₈H₁₈Cl₂N₄O₃
Molecular Weight:409.272
Hs Code.:

Synonyms:1-(4-Chloro-phenyl)-3-[3-(4-chloro-phenyl)-4-hydroxy-5,5-dimethyl-2-oxo-imidazolidin-1-yl]-urea

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Chemical Property of 1-(4-Chloro-phenyl)-3-[3-(4-chloro-phenyl)-4-hydroxy-5,5-dimethyl-2-oxo-imidazolidin-1-yl]-urea

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Technology Process of 1-(4-Chloro-phenyl)-3-[3-(4-chloro-phenyl)-4-hydroxy-5,5-dimethyl-2-oxo-imidazolidin-1-yl]-urea

There total 3 articles about 1-(4-Chloro-phenyl)-3-[3-(4-chloro-phenyl)-4-hydroxy-5,5-dimethyl-2-oxo-imidazolidin-1-yl]-urea 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: 84.0%

: 85601-61-2
C₁₈H₁₉Cl₂N₅O₃

: 85601-71-4
1-(4-Chloro-phenyl)-3-[3-(4-chloro-phenyl)-4-hydroxy-5,5-dimethyl-2-oxo-imidazolidin-1-yl]-urea

Guidance literature:: With sulfuric acid; In ethanol;
DOI:10.1007/BF00512820

Reference yield:

: 104-12-1
p-chlorphenylisocyanate

: 85601-71-4
1-(4-Chloro-phenyl)-3-[3-(4-chloro-phenyl)-4-hydroxy-5,5-dimethyl-2-oxo-imidazolidin-1-yl]-urea

Guidance literature:: Multi-step reaction with 3 steps

1: 60 percent / dioxane / 1 h

2: 94 percent / dioxane / 0.17 h

3: 84 percent / H₂SO₄ / ethanol

With sulfuric acid; In 1,4-dioxane; ethanol;
DOI:10.1007/BF00512820

Reference yield:

: 85601-49-6
C₁₁H₁₅ClN₄O₂

: 85601-71-4
1-(4-Chloro-phenyl)-3-[3-(4-chloro-phenyl)-4-hydroxy-5,5-dimethyl-2-oxo-imidazolidin-1-yl]-urea

Guidance literature:: Multi-step reaction with 2 steps

1: 94 percent / dioxane / 0.17 h

2: 84 percent / H₂SO₄ / ethanol

With sulfuric acid; In 1,4-dioxane; ethanol;
DOI:10.1007/BF00512820