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

Base Information

Chemical Name:(E)-2-(4-(1-(((5-methyl-2-phenyloxazol-4-yl)methoxy)imino)propyl)phenoxy)acetic acid
CAS No.:1268705-42-5
Molecular Formula:C₂₂H₂₂N₂O₅
Molecular Weight:394.427
Hs Code.:

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

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

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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

Chemical Property:

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

There total 5 articles about (E)-2-(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: 80.0%

: 1268705-30-1
(E)-ethyl 2-(4-(1-(((5-methyl-2-phenyloxazol-4-yl)methoxy)imino)propyl)phenoxy)acetate

: 1268705-42-5
(E)-2-(4-(1-(((5-methyl-2-phenyloxazol-4-yl)methoxy)imino)propyl)phenoxy)acetic acid

Guidance literature:: With lithium hydroxide monohydrate; water; In tetrahydrofuran; methanol; at 20 ℃; for 18h;
DOI:10.1016/j.bmc.2010.12.023

Reference yield:

: 1268705-07-2
(E)-ethyl 2-(4-(1-(hydroxyimino)propyl)phenoxy)acetate

: 1268705-42-5
(E)-2-(4-(1-(((5-methyl-2-phenyloxazol-4-yl)methoxy)imino)propyl)phenoxy)acetic acid

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

Reference yield:

: 637-27-4,132899-52-6
phenyl propionate

: 1268705-42-5
(E)-2-(4-(1-(((5-methyl-2-phenyloxazol-4-yl)methoxy)imino)propyl)phenoxy)acetic acid

Guidance literature:: Multi-step reaction with 5 steps

1: aluminum (III) chloride / 2 h / 25 - 165 °C

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

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

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

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

With aluminum (III) chloride; lithium hydroxide monohydrate; hydroxylamine hydrochloride; water; sodium acetate; potassium carbonate; caesium carbonate; In tetrahydrofuran; methanol; ethanol; water; N,N-dimethyl-formamide;
DOI:10.1016/j.bmc.2010.12.023