1-bromo-2-(2-iodoethyl)-5-methoxy-4-(1-methylethoxy)benzene

Base Information

• Chemical Name: 1-bromo-2-(2-iodoethyl)-5-methoxy-4-(1-methylethoxy)benzene
• CAS No.: 365572-24-3
• Molecular Formula: C₁₂H₁₆BrIO₂
• Molecular Weight: 399.066
• Mol file: 365572-24-3.mol

Synonyms:1-bromo-2-(2-iodoethyl)-5-methoxy-4-(1-methylethoxy)benzene

Chemical Property of 1-bromo-2-(2-iodoethyl)-5-methoxy-4-(1-methylethoxy)benzene

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 1-bromo-2-(2-iodoethyl)-5-methoxy-4-(1-methylethoxy)benzene

There total 4 articles about 1-bromo-2-(2-iodoethyl)-5-methoxy-4-(1-methylethoxy)benzene 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: 77.0%

2-(2-bromo-4-methoxy-5-(1-methylethoxy)benzene)ethanol (365572-23-2) → 1-bromo-2-(2-iodoethyl)-5-methoxy-4-(1-methylethoxy)benzene (365572-24-3)

Guidance literature:

With 1H-imidazole; iodine; triphenylphosphine; In dichloromethane; at 20 ℃; for 2h;

DOI:10.3390/70400374

Reference yield:

2-bromo-4-methoxy-5-(1-methylethoxy)benzeneacetaldehyde (365572-22-1) → 1-bromo-2-(2-iodoethyl)-5-methoxy-4-(1-methylethoxy)benzene (365572-24-3)

Guidance literature:

Multi-step reaction with 2 steps

1: 99 percent / sodium borohydride / ethanol / 2 h / 15 °C

2: 77 percent / imidazole; iodine; triphenylphosphine / CH₂Cl₂ / 2 h / 20 °C

With 1H-imidazole; sodium tetrahydroborate; iodine; triphenylphosphine; In ethanol; dichloromethane;

DOI:10.3390/70400374

Reference yield:

1-bromo-5-methoxy-2-(2-methoxyethenyl)-4-(1-methylethoxy)benzene → 1-bromo-2-(2-iodoethyl)-5-methoxy-4-(1-methylethoxy)benzene (365572-24-3)

Guidance literature:

Multi-step reaction with 3 steps

1: 98 percent / hydrochloric acid / tetrahydrofuran / 3 h / Heating

2: 99 percent / sodium borohydride / ethanol / 2 h / 15 °C

3: 77 percent / imidazole; iodine; triphenylphosphine / CH₂Cl₂ / 2 h / 20 °C

With 1H-imidazole; hydrogenchloride; sodium tetrahydroborate; iodine; triphenylphosphine; In tetrahydrofuran; ethanol; dichloromethane;

DOI:10.3390/70400374

upstream raw materials:

2-(2-bromo-4-methoxy-5-(1-methylethoxy)benzene)ethanol

2-bromo-4-methoxy-5-(1-methylethoxy)benzeneacetaldehyde

Downstream raw materials:

2-[2-[2-bromo-4-methoxy-5-(1-methylethoxy)phenyl]ethyl]-2-[4-(1-methylethoxy)phenylmethyl]propane-1,3-dicarboxylic acid dimethyl ester

4-(2-bromo-5-isopropoxy-4-methoxy-phenyl)-2-(4-isopropoxy-benzyl)-butyric acid

4-(2-bromo-5-isopropoxy-4-methoxy-phenyl)-2-(4-isopropoxy-benzyl)-butyramide

4-(2-bromo-5-hydroxy-4-methoxy-phenyl)-2-(4-hydroxy-benzyl)-butyramide