(4-ethoxycarbonylmethoxy-2,3,5,6-tetrafluoro-phenoxy)-acetic acid ethyl ester

Base Information

• Chemical Name: (4-ethoxycarbonylmethoxy-2,3,5,6-tetrafluoro-phenoxy)-acetic acid ethyl ester
• CAS No.: 864847-43-8
• Molecular Formula: C₁₄H₁₄F₄O₆
• Molecular Weight: 354.255
• Mol file: 864847-43-8.mol

Synonyms:(4-ethoxycarbonylmethoxy-2,3,5,6-tetrafluoro-phenoxy)-acetic acid ethyl ester

Chemical Property of (4-ethoxycarbonylmethoxy-2,3,5,6-tetrafluoro-phenoxy)-acetic acid ethyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
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MSDS Files:

Useful:

Technology Process of (4-ethoxycarbonylmethoxy-2,3,5,6-tetrafluoro-phenoxy)-acetic acid ethyl ester

There total 1 articles about (4-ethoxycarbonylmethoxy-2,3,5,6-tetrafluoro-phenoxy)-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: 67.0%

2,3,5,6-tetrafluoro-1,4-benzenediol (771-63-1) + ethyl bromoacetate (105-36-2) → (4-ethoxycarbonylmethoxy-2,3,5,6-tetrafluoro-phenoxy)-acetic acid ethyl ester (864847-43-8)

Guidance literature:

With potassium carbonate; In tetrahydrofuran; Heating;

DOI:10.1039/b506883e

Reference yield: 93.0%

(4-ethoxycarbonylmethoxy-2,3,5,6-tetrafluoro-phenoxy)-acetic acid ethyl ester (864847-43-8) → (4-carboxymethoxy-2,3,5,6-tetrafluoro-phenoxy)-acetic acid (864847-44-9)

Guidance literature:

With sodium hydroxide; In tetrahydrofuran; ethanol; at 20 ℃;

DOI:10.1039/b506883e

Reference yield:

(4-ethoxycarbonylmethoxy-2,3,5,6-tetrafluoro-phenoxy)-acetic acid ethyl ester (864847-43-8) → (4-chlorocarbonylmethoxy-2,3,5,6-tetrafluoro-phenoxy)-acetyl chloride (864847-45-0)

Guidance literature:

Multi-step reaction with 2 steps

1: 93 percent / NaOH / ethanol; tetrahydrofuran / 20 °C

2: 100 percent / SOCl₂ / Heating

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

DOI:10.1039/b506883e

upstream raw materials:

2,3,5,6-tetrafluoro-1,4-benzenediol

ethyl bromoacetate

Downstream raw materials:

(4-carboxymethoxy-2,3,5,6-tetrafluoro-phenoxy)-acetic acid

(4-chlorocarbonylmethoxy-2,3,5,6-tetrafluoro-phenoxy)-acetyl chloride