2-(4-bromophenoxy)-N-[(4-iodophenylcarbamoyl)methyl]acetamide

Base Information

• Chemical Name: 2-(4-bromophenoxy)-N-[(4-iodophenylcarbamoyl)methyl]acetamide
• CAS No.: 1448523-92-9
• Molecular Formula: C₁₆H₁₄BrIN₂O₃
• Molecular Weight: 489.107
• Mol file: 1448523-92-9.mol

Synonyms:2-(4-bromophenoxy)-N-[(4-iodophenylcarbamoyl)methyl]acetamide

Chemical Property of 2-(4-bromophenoxy)-N-[(4-iodophenylcarbamoyl)methyl]acetamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 2-(4-bromophenoxy)-N-[(4-iodophenylcarbamoyl)methyl]acetamide

There total 6 articles about 2-(4-bromophenoxy)-N-[(4-iodophenylcarbamoyl)methyl]acetamide 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-amino-N-(4-iodophenyl)acetamide (855594-21-7) + C11H9BrN2O2 (110009-65-9) → 2-(4-bromophenoxy)-N-[(4-iodophenylcarbamoyl)methyl]acetamide (1448523-92-9)

Guidance literature:

In dichloromethane; at 20 ℃; for 24h;

DOI:10.1016/j.bmcl.2014.07.003

Reference yield:

(4-bromophenoxy)acetic acid methyl ester (4841-23-0) → 2-(4-bromophenoxy)-N-[(4-iodophenylcarbamoyl)methyl]acetamide (1448523-92-9)

Guidance literature:

Multi-step reaction with 3 steps

1: lithium hydroxide monohydrate / methanol; water / 2 h / Reflux

2: dichloromethane / 1 h / 20 °C

3: dichloromethane / 24 h / 20 °C

With lithium hydroxide monohydrate; In methanol; dichloromethane; water;

DOI:10.1016/j.bmcl.2014.07.003

Reference yield:

[(4-iodophenylcarbamoyl)methyl]carbamic acid tert-butyl ester (216774-64-0) → 2-(4-bromophenoxy)-N-[(4-iodophenylcarbamoyl)methyl]acetamide (1448523-92-9)

Guidance literature:

Multi-step reaction with 2 steps

1: trifluoroacetic acid / dichloromethane / 24 h / 20 °C

2: dichloromethane / 24 h / 20 °C

With trifluoroacetic acid; In dichloromethane;

DOI:10.1016/j.bmcl.2014.07.003

upstream raw materials:

2-amino-N-(4-iodophenyl)acetamide

C₁₁H₉BrN₂O₂

[(4-iodophenylcarbamoyl)methyl]carbamic acid tert-butyl ester

(4-bromophenoxy)acetic acid methyl ester