ethyl 2-(3-bromo-5-chloro-4-(2,2,2-trifluoroethoxy)phenyl)acetate

Base Information

• Chemical Name: ethyl 2-(3-bromo-5-chloro-4-(2,2,2-trifluoroethoxy)phenyl)acetate
• CAS No.: 1168134-12-0
• Molecular Formula: C₁₂H₁₁BrClF₃O₃
• Molecular Weight: 375.57
• Mol file: 1168134-12-0.mol

Synonyms:ethyl 2-(3-bromo-5-chloro-4-(2,2,2-trifluoroethoxy)phenyl)acetate

Chemical Property of ethyl 2-(3-bromo-5-chloro-4-(2,2,2-trifluoroethoxy)phenyl)acetate

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of ethyl 2-(3-bromo-5-chloro-4-(2,2,2-trifluoroethoxy)phenyl)acetate

There total 4 articles about ethyl 2-(3-bromo-5-chloro-4-(2,2,2-trifluoroethoxy)phenyl)acetate 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: 43.0%

1,1,1-trifluoro-2-iodoethane (353-83-3) + ethyl 2-(3-bromo-5-chloro-4-hydroxyphenyl)acetate (1168133-68-3) → ethyl 2-(3-bromo-5-chloro-4-(2,2,2-trifluoroethoxy)phenyl)acetate (1168134-12-0)

Guidance literature:

With potassium carbonate; In N,N-dimethyl-formamide; at 20 - 100 ℃; for 24h;

Reference yield: 30.0%

1,1,1-trifluoro-2-iodoethane (353-83-3) + 3-chloro-4-hydroxyphenylacetic acid ethyl ester (193357-36-7) → ethyl 2-(3-bromo-5-chloro-4-(2,2,2-trifluoroethoxy)phenyl)acetate (1168134-12-0)

Guidance literature:

With potassium carbonate; In N,N-dimethyl-formamide; at 20 - 100 ℃;

Reference yield:

3-chloro-4-hydroxyphenylacetic acid ethyl ester (193357-36-7) → ethyl 2-(3-bromo-5-chloro-4-(2,2,2-trifluoroethoxy)phenyl)acetate (1168134-12-0)

Guidance literature:

Multi-step reaction with 2 steps

1: bromine / tetrachloromethane / 1.5 h / -10 °C

2: potassium carbonate / N,N-dimethyl-formamide / 24 h / 20 - 100 °C

With bromine; potassium carbonate; In tetrachloromethane; N,N-dimethyl-formamide;

upstream raw materials:

1,1,1-trifluoro-2-iodoethane

3-chloro-4-hydroxyphenylacetic acid ethyl ester

ethyl 2-(3-bromo-5-chloro-4-hydroxyphenyl)acetate

ethyl 2-(3-bromo-4-hydroxyphenyl)acetate

Downstream raw materials:

ethyl 2-(3-bromo-5-chloro-4-(2,2,2-trifluoroethoxy)phenyl)-3-cyclopropylpropanoate

ethyl 1-(3-bromo-5-chloro-4-(2,2,2-trifluoroethoxy)phenyl)cyclobutanecarboxylate

ethyl 1-(5-chloro-6-(2,2,2-trifluoroethoxy)-4'-(trifluoromethyl)biphenyl-3-yl)cyclobutane carboxylate

1-(5-chloro-6-(2,2,2-trifluoroethoxy)-4'-(trifluoromethyl)biphenyl-3-yl)cyclobutane carboxylic acid