(E)-benzyl 2-(4-methoxy-3-(3-methoxypropoxy)benzylidene)-3-methylbutanoate

Base Information

• Chemical Name: (E)-benzyl 2-(4-methoxy-3-(3-methoxypropoxy)benzylidene)-3-methylbutanoate
• CAS No.: 1431617-54-7
• Molecular Formula: C₂₄H₃₀O₅
• Molecular Weight: 398.499
• Mol file: 1431617-54-7.mol

Synonyms:(E)-benzyl 2-(4-methoxy-3-(3-methoxypropoxy)benzylidene)-3-methylbutanoate

Chemical Property of (E)-benzyl 2-(4-methoxy-3-(3-methoxypropoxy)benzylidene)-3-methylbutanoate

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

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Technology Process of (E)-benzyl 2-(4-methoxy-3-(3-methoxypropoxy)benzylidene)-3-methylbutanoate

There total 1 articles about (E)-benzyl 2-(4-methoxy-3-(3-methoxypropoxy)benzylidene)-3-methylbutanoate 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:

C17H23ClO4 + benzyl alcohol (100-51-6,185532-71-2) → (E)-benzyl 2-(4-methoxy-3-(3-methoxypropoxy)benzylidene)-3-methylbutanoate (1431617-54-7)

Guidance literature:

In dichloromethane; at 20 ℃;

DOI:10.1002/chem.201202397

Reference yield:

(E)-benzyl 2-(4-methoxy-3-(3-methoxypropoxy)benzylidene)-3-methylbutanoate (1431617-54-7) → C24H32O5

Guidance literature:

With C₃₂H₁₂BF₂₄^(1-)*C₄₁H₄₇IrN₂P⁽¹⁺⁾; hydrogen; In dichloromethane; at 20 ℃; for 2h; under 37503.8 Torr; enantioselective reaction; Autoclave;

DOI:10.1002/chem.201202397

Reference yield:

(E)-benzyl 2-(4-methoxy-3-(3-methoxypropoxy)benzylidene)-3-methylbutanoate (1431617-54-7) → C24H32O5 + C24H32O5

Guidance literature:

With C₃₂H₁₂BF₂₄^(1-)*C₃₃H₅₀IrNOP⁽¹⁺⁾; hydrogen; In dichloromethane; at 20 ℃; for 2h; under 37503.8 Torr; Reagent/catalyst; enantioselective reaction; Autoclave;

DOI:10.1002/chem.201202397

upstream raw materials:

benzyl alcohol