N-{(E)-3-ethoxy-4-[(3-methyl-1,2-oxazol-5-yl)methoxy]benzylidene}-4-phenoxyaniline

Base Information

Chemical Name:N-{(E)-3-ethoxy-4-[(3-methyl-1,2-oxazol-5-yl)methoxy]benzylidene}-4-phenoxyaniline
CAS No.:1482447-99-3
Molecular Formula:C₂₆H₂₄N₂O₄
Molecular Weight:428.488
Hs Code.:

Synonyms:N-{(E)-3-ethoxy-4-[(3-methyl-1,2-oxazol-5-yl)methoxy]benzylidene}-4-phenoxyaniline

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Chemical Property of N-{(E)-3-ethoxy-4-[(3-methyl-1,2-oxazol-5-yl)methoxy]benzylidene}-4-phenoxyaniline

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Technology Process of N-{(E)-3-ethoxy-4-[(3-methyl-1,2-oxazol-5-yl)methoxy]benzylidene}-4-phenoxyaniline

There total 3 articles about N-{(E)-3-ethoxy-4-[(3-methyl-1,2-oxazol-5-yl)methoxy]benzylidene}-4-phenoxyaniline 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: 81.0%

: 1042775-50-7
3-ethoxy-4-[(3-methyl-1,2-oxazol-5-yl)methoxy]benzaldehyde

: 139-59-3
4-phenoxyanilin

: 1482447-99-3
N-{(E)-3-ethoxy-4-[(3-methyl-1,2-oxazol-5-yl)methoxy]benzylidene}-4-phenoxyaniline

Guidance literature:: In methanol; Reflux;
DOI:10.1134/S1070428013100199

Reference yield:

: 40340-41-8
5-chloromethyl-3-methylisoxazole

: 1482447-99-3
N-{(E)-3-ethoxy-4-[(3-methyl-1,2-oxazol-5-yl)methoxy]benzylidene}-4-phenoxyaniline

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / ethanol / 12 h / 70 °C / Inert atmosphere

2: methanol / Reflux

With potassium carbonate; In methanol; ethanol; 1: |Williamson Ether Synthesis;
DOI:10.1134/S1070428013100199

Reference yield:

: 121-32-4
4-hydroxy-3-ethoxybenzaldehyde

: 1482447-99-3
N-{(E)-3-ethoxy-4-[(3-methyl-1,2-oxazol-5-yl)methoxy]benzylidene}-4-phenoxyaniline

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / ethanol / 12 h / 70 °C / Inert atmosphere

2: methanol / Reflux

With potassium carbonate; In methanol; ethanol; 1: |Williamson Ether Synthesis;
DOI:10.1134/S1070428013100199