[3-(4-Chloro-benzyl)-2,4,5-trioxo-imidazolidin-1-yl]-acetic acid ethyl ester

Base Information

• Chemical Name: [3-(4-Chloro-benzyl)-2,4,5-trioxo-imidazolidin-1-yl]-acetic acid ethyl ester
• CAS No.: 128043-68-5
• Molecular Formula: C₁₄H₁₃ClN₂O₅
• Molecular Weight: 324.721
• Mol file: 128043-68-5.mol

Synonyms:[3-(4-Chloro-benzyl)-2,4,5-trioxo-imidazolidin-1-yl]-acetic acid ethyl ester

Chemical Property of [3-(4-Chloro-benzyl)-2,4,5-trioxo-imidazolidin-1-yl]-acetic acid ethyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of [3-(4-Chloro-benzyl)-2,4,5-trioxo-imidazolidin-1-yl]-acetic acid ethyl ester

There total 2 articles about [3-(4-Chloro-benzyl)-2,4,5-trioxo-imidazolidin-1-yl]-acetic acid ethyl ester 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:

(4-chlorophenyl)methanamine hydrochloride (42365-43-5) → [3-(4-Chloro-benzyl)-2,4,5-trioxo-imidazolidin-1-yl]-acetic acid ethyl ester (128043-68-5)

Guidance literature:

Multi-step reaction with 3 steps

1: conc. HCl / H₂O / 3 h / Heating

2: tetrahydrofuran / 3 h / Ambient temperature

3: KOH / ethanol / 8 h / Heating

With hydrogenchloride; potassium hydroxide; In tetrahydrofuran; ethanol; water;

DOI:10.1021/jm9508393

Reference yield:

N-(4-chlorobenzyl)urea (65608-74-4) → [3-(4-Chloro-benzyl)-2,4,5-trioxo-imidazolidin-1-yl]-acetic acid ethyl ester (128043-68-5)

Guidance literature:

Multi-step reaction with 2 steps

1: tetrahydrofuran / 3 h / Ambient temperature

2: KOH / ethanol / 8 h / Heating

With potassium hydroxide; In tetrahydrofuran; ethanol;

DOI:10.1021/jm9508393

Reference yield:

[3-(4-Chloro-benzyl)-2,4,5-trioxo-imidazolidin-1-yl]-acetic acid ethyl ester (128043-68-5) → 3-Carboxymethyl-1-(4-chlorobenzyl)parabanic acid

Guidance literature:

With hydrogenchloride; acetic acid; for 4.5h; Heating;

DOI:10.1021/jm9508393

upstream raw materials:

N-(4-chlorobenzyl)urea

(4-chlorophenyl)methanamine hydrochloride