(E)-2-(2-methyl-4-(1-(((5-methyl-2-phenyloxazol-4-yl)methoxy)imino)propyl)phenoxy)acetic acid

Base Information

• Chemical Name: (E)-2-(2-methyl-4-(1-(((5-methyl-2-phenyloxazol-4-yl)methoxy)imino)propyl)phenoxy)acetic acid
• CAS No.: 1268705-41-4
• Molecular Formula: C₂₃H₂₄N₂O₅
• Molecular Weight: 408.454
• Mol file: 1268705-41-4.mol

Synonyms:(E)-2-(2-methyl-4-(1-(((5-methyl-2-phenyloxazol-4-yl)methoxy)imino)propyl)phenoxy)acetic acid

Chemical Property of (E)-2-(2-methyl-4-(1-(((5-methyl-2-phenyloxazol-4-yl)methoxy)imino)propyl)phenoxy)acetic acid

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (E)-2-(2-methyl-4-(1-(((5-methyl-2-phenyloxazol-4-yl)methoxy)imino)propyl)phenoxy)acetic acid

There total 5 articles about (E)-2-(2-methyl-4-(1-(((5-methyl-2-phenyloxazol-4-yl)methoxy)imino)propyl)phenoxy)acetic acid 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: 85.0%

(E)-ethyl 2-(2-methyl-4-(1-(((5-methyl-2-phenyloxazol-4-yl)methoxy)imino)propyl)phenoxy)acetate (1268705-28-7) → (E)-2-(2-methyl-4-(1-(((5-methyl-2-phenyloxazol-4-yl)methoxy)imino)propyl)phenoxy)acetic acid (1268705-41-4)

Guidance literature:

With lithium hydroxide monohydrate; water; In tetrahydrofuran; methanol; at 20 ℃; for 18h;

DOI:10.1016/j.bmc.2010.12.023

Reference yield:

ethyl 2-(2-methyl-4-propionylphenoxy)acetate (1268704-95-5) → (E)-2-(2-methyl-4-(1-(((5-methyl-2-phenyloxazol-4-yl)methoxy)imino)propyl)phenoxy)acetic acid (1268705-41-4)

Guidance literature:

Multi-step reaction with 3 steps

1: hydroxylamine hydrochloride; sodium acetate / ethanol; water / 1 h / Reflux

2: caesium carbonate / N,N-dimethyl-formamide / 18 h / 60 °C

3: lithium hydroxide monohydrate; water / tetrahydrofuran; methanol / 18 h / 20 °C

With lithium hydroxide monohydrate; hydroxylamine hydrochloride; water; sodium acetate; caesium carbonate; In tetrahydrofuran; methanol; ethanol; water; N,N-dimethyl-formamide;

DOI:10.1016/j.bmc.2010.12.023

Reference yield:

(E)-ethyl 2-(4-(1-(hydroxyimino)propyl)-2-methylphenoxy)acetate (1268705-04-9) → (E)-2-(2-methyl-4-(1-(((5-methyl-2-phenyloxazol-4-yl)methoxy)imino)propyl)phenoxy)acetic acid (1268705-41-4)

Guidance literature:

Multi-step reaction with 2 steps

1: caesium carbonate / N,N-dimethyl-formamide / 18 h / 60 °C

2: lithium hydroxide monohydrate; water / tetrahydrofuran; methanol / 18 h / 20 °C

With lithium hydroxide monohydrate; water; caesium carbonate; In tetrahydrofuran; methanol; N,N-dimethyl-formamide;

DOI:10.1016/j.bmc.2010.12.023

upstream raw materials:

ethyl 2-(2-methyl-4-propionylphenoxy)acetate

(E)-ethyl 2-(4-(1-(hydroxyimino)propyl)-2-methylphenoxy)acetate

(E)-ethyl 2-(2-methyl-4-(1-(((5-methyl-2-phenyloxazol-4-yl)methoxy)imino)propyl)phenoxy)acetate

1-(4-hydroxy-3-methylphenyl)propan-1-one