N-<2-(2-bromo-4,5-dimethoxy)phenyl>ethyl(2-iodophenyl)acetamide

Base Information

• Chemical Name: N-<2-(2-bromo-4,5-dimethoxy)phenyl>ethyl(2-iodophenyl)acetamide
• CAS No.: 238740-84-6
• Molecular Formula: C₁₈H₁₉BrINO₃
• Molecular Weight: 504.162
• Mol file: 238740-84-6.mol

Synonyms:N-<2-(2-bromo-4,5-dimethoxy)phenyl>ethyl(2-iodophenyl)acetamide

Chemical Property of N-<2-(2-bromo-4,5-dimethoxy)phenyl>ethyl(2-iodophenyl)acetamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of N-<2-(2-bromo-4,5-dimethoxy)phenyl>ethyl(2-iodophenyl)acetamide

There total 5 articles about N-<2-(2-bromo-4,5-dimethoxy)phenyl>ethyl(2-iodophenyl)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: 91.0%

o-iodophenylacetyl chloride (62300-07-6) + 2-(2-bromo-4,5-dimethoxyphenylphenyl)ethan-1-amine (63375-81-5) → N-<2-(2-bromo-4,5-dimethoxy)phenyl>ethyl(2-iodophenyl)acetamide (238740-84-6)

Guidance literature:

With triethylamine; In tetrahydrofuran; for 12h; Ambient temperature;

DOI:10.1021/jo9901900

Reference yield:

2-(2-iodophenyl)acetonitrile (40400-15-5) → N-<2-(2-bromo-4,5-dimethoxy)phenyl>ethyl(2-iodophenyl)acetamide (238740-84-6)

Guidance literature:

Multi-step reaction with 3 steps

1: 87 percent / NaOH / ethanol; H₂O / 6.5 h / Heating

2: 2.60 g / SOCl₂ / 12 h / Ambient temperature

3: 91 percent / Et₃N / tetrahydrofuran / 12 h / Ambient temperature

With sodium hydroxide; thionyl chloride; triethylamine; In tetrahydrofuran; ethanol; water;

DOI:10.1021/jo9901900

Reference yield:

o-iodophenylacetic acid (18698-96-9) → N-<2-(2-bromo-4,5-dimethoxy)phenyl>ethyl(2-iodophenyl)acetamide (238740-84-6)

Guidance literature:

Multi-step reaction with 2 steps

1: 2.60 g / SOCl₂ / 12 h / Ambient temperature

2: 91 percent / Et₃N / tetrahydrofuran / 12 h / Ambient temperature

With thionyl chloride; triethylamine; In tetrahydrofuran;

DOI:10.1021/jo9901900

upstream raw materials:

o-iodophenylacetyl chloride

2-(2-bromo-4,5-dimethoxyphenylphenyl)ethan-1-amine

2-(2-iodophenyl)acetonitrile

o-iodophenylacetic acid