(Z)-3-(3,4,5-Tris-benzyloxy-phenyl)-acrylic acid ethyl ester

Base Information

• Chemical Name: (Z)-3-(3,4,5-Tris-benzyloxy-phenyl)-acrylic acid ethyl ester
• CAS No.: 524004-55-5
• Molecular Formula: C₃₂H₃₀O₅
• Molecular Weight: 494.587
• Mol file: 524004-55-5.mol

Synonyms:(Z)-3-(3,4,5-Tris-benzyloxy-phenyl)-acrylic acid ethyl ester

Chemical Property of (Z)-3-(3,4,5-Tris-benzyloxy-phenyl)-acrylic acid ethyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (Z)-3-(3,4,5-Tris-benzyloxy-phenyl)-acrylic acid ethyl ester

There total 8 articles about (Z)-3-(3,4,5-Tris-benzyloxy-phenyl)-acrylic 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: 100.0%

diethoxyphosphoryl-acetic acid ethyl ester (867-13-0) + 3,4,5-tribenzyloxybenzaldehyde (6137-86-6) → (Z)-3-(3,4,5-Tris-benzyloxy-phenyl)-acrylic acid ethyl ester (524004-55-5)

Guidance literature:

With sodium hydride; In tetrahydrofuran; at 0 - 20 ℃; Inert atmosphere;

Reference yield: 91.0%

3,4,5-tribenzyloxybenzaldehyde (6137-86-6) + ethyl (triphenylphosphoranylidene)acetate (1099-45-2) → (Z)-3-(3,4,5-Tris-benzyloxy-phenyl)-acrylic acid ethyl ester (524004-55-5)

Guidance literature:

In benzene; at 25 ℃;

DOI:10.1081/SCC-120013726

Reference yield:

3,4,5-trihydroxybenzoic acid (149-91-7) → (Z)-3-(3,4,5-Tris-benzyloxy-phenyl)-acrylic acid ethyl ester (524004-55-5)

Guidance literature:

Multi-step reaction with 5 steps

1: 81 percent / H₂SO₄

2: 95 percent / K₂CO₃ / acetone / 5 h / 50 °C

3: 92 percent / LiAlH₄

4: 87 percent / C₅H₅*CrO₃*HCl / CH₂Cl₂ / 0 °C

5: 91 percent / benzene / 25 °C

With lithium aluminium tetrahydride; C₅H₅*CrO₃*HCl; sulfuric acid; potassium carbonate; In dichloromethane; acetone; benzene; 5: Wittig reaction;

DOI:10.1081/SCC-120013726

upstream raw materials:

3,4,5-tribenzyloxybenzaldehyde

ethyl (triphenylphosphoranylidene)acetate

3,4,5-trihydroxybenzoic acid

methyl galloate

Downstream raw materials:

3-(3,4,5-tris(benzyloxy)phenyl)propan-1-ol

5-(3-hydroxypropyl)benzene-1,2,3-triol

1,2,3-Tris-benzyloxy-5-(3-bromo-propyl)-benzene

C₃₀H₂₈O₄