(E)-3-[4-(5-Methyl-2-phenyl-oxazol-4-ylmethoxy)-phenyl]-acrylic acid methyl ester

Base Information

Chemical Name:(E)-3-[4-(5-Methyl-2-phenyl-oxazol-4-ylmethoxy)-phenyl]-acrylic acid methyl ester
CAS No.:1027950-64-6
Molecular Formula:C₂₁H₁₉NO₄
Molecular Weight:349.386
Hs Code.:

Synonyms:(E)-3-[4-(5-Methyl-2-phenyl-oxazol-4-ylmethoxy)-phenyl]-acrylic acid methyl ester

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Chemical Property of (E)-3-[4-(5-Methyl-2-phenyl-oxazol-4-ylmethoxy)-phenyl]-acrylic acid methyl ester

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Technology Process of (E)-3-[4-(5-Methyl-2-phenyl-oxazol-4-ylmethoxy)-phenyl]-acrylic acid methyl ester

There total 1 articles about (E)-3-[4-(5-Methyl-2-phenyl-oxazol-4-ylmethoxy)-phenyl]-acrylic acid methyl 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:

: 5927-18-4
trimethyl phosphonoacetate

: 103789-66-8
4-(5-methyl-2-phenyl-4-oxazolylmethoxy)-benzaldehyde

: 1027950-64-6
(E)-3-[4-(5-Methyl-2-phenyl-oxazol-4-ylmethoxy)-phenyl]-acrylic acid methyl ester

Guidance literature:: With sodium methylate; In methanol; at 0 ℃; for 2h;
DOI:10.1021/jm010490l

Reference yield:

: 1027950-64-6
(E)-3-[4-(5-Methyl-2-phenyl-oxazol-4-ylmethoxy)-phenyl]-acrylic acid methyl ester

: 159017-64-8
(E)-3-[4-(5-methyl-2-phenyl-4-oxazolylmethoxy)phenyl]-2-propen-1-ol

Guidance literature:: With diisobutylaluminium hydride; In dichloromethane; toluene; at 0 - 20 ℃; for 1.5h;
DOI:10.1021/jm010490l

Reference yield:

: 1027950-64-6
(E)-3-[4-(5-Methyl-2-phenyl-oxazol-4-ylmethoxy)-phenyl]-acrylic acid methyl ester

: 5-[3-[4-(5-methyl-2-phenyl-4-oxazolylmethoxy)phenyl]propyl]-2,4-oxazolidinedione

Guidance literature:: Multi-step reaction with 4 steps

1: diisobutylaluminum hydride / CH₂Cl₂; toluene / 1.5 h / 0 - 20 °C

2: 70 percent / MnO₂ / CH₂Cl₂ / 14 h / 20 °C

3: 26 percent / piperidine / ethanol / 3 h / Heating

4: H₂ / 5percent Pd/C / dioxane; ethanol / atmospheric pressure

With piperidine; manganese(IV) oxide; hydrogen; diisobutylaluminium hydride; 5percent Pd/C; In 1,4-dioxane; ethanol; dichloromethane; toluene;
DOI:10.1021/jm010490l