Acetic acid, [(4-methoxyphenyl)imino]-, ethyl ester

Base Information

• Chemical Name: Acetic acid, [(4-methoxyphenyl)imino]-, ethyl ester
• CAS No.: 115276-75-0
• Molecular Formula: C₁₁H₁₃NO₃
• Molecular Weight: 207.229
• DSSTox Substance ID: DTXSID10450890
• Nikkaji Number: J1.153.432E,J2.411.979C
• Mol file: 115276-75-0.mol

Synonyms:115276-75-0;Acetic acid, [(4-methoxyphenyl)imino]-, ethyl ester;SCHEMBL809447;SCHEMBL12528504;DTXSID10450890;SZATXVFGSXZJHE-WQLSENKSSA-N;Ethyl (4-methoxyphenylimino)acetate;(Z)-ethyl 2-(4-methoxyphenylimino)acetate;ethyl (2E)-2-(4-methoxyphenyl)iminoacetate;ethyl (2E)-[(4-methoxyphenyl)imino]ethanoate;[(E)-(4-Methoxyphenyl)imino]acetic acid ethyl ester

Chemical Property of Acetic acid, [(4-methoxyphenyl)imino]-, ethyl ester

Chemical Property:

• XLogP3: 2.2
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 5
• Exact Mass: 207.08954328
• Heavy Atom Count: 15
• Complexity: 220

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCOC(=O)C=NC1=CC=C(C=C1)OC

Technology Process of Acetic acid, [(4-methoxyphenyl)imino]-, ethyl ester

There total 7 articles about Acetic acid, [(4-methoxyphenyl)imino]-, ethyl 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: 100.0%

glyoxylic acid ethyl ester (924-44-7) + 4-methoxy-aniline (104-94-9) → ethyl (E)-2-(p-methoxyphenylimino)acetate (115276-75-0,124156-21-4,120419-96-7)

Guidance literature:

With silica gel; In dichloromethane; toluene; for 20h; sonication;

DOI:10.1021/jo062406l

Reference yield: 93.0%

N-(4-methoxy)phenylglycine ethyl ester (50845-77-7) → ethyl (E)-2-(p-methoxyphenylimino)acetate (115276-75-0,124156-21-4,120419-96-7)

Guidance literature:

With manganese(IV) oxide; In dichloromethane; at 20 ℃; for 1h; Inert atmosphere;

DOI:10.1248/cpb.c17-00158

Reference yield:

C4H8O3 + 4-methoxy-aniline (104-94-9) → ethyl (E)-2-(p-methoxyphenylimino)acetate (115276-75-0,124156-21-4,120419-96-7)

Guidance literature:

With sodium sulfate; for 1.25h; Milling;

DOI:10.3390/molecules26051330

upstream raw materials:

glyoxylic acid ethyl ester

4-methoxy-aniline

oxalic acid monoethyl ester

N-(4-methoxy)phenylglycine ethyl ester

Downstream raw materials:

ethyl (S)-2-(4-methoxyphenylamino)-2-((S)-2-oxocyclohexyl)-acetate

(2S)-ethyl 2-(p-methoxyphenylamino)-4-oxo-pentanoate

ethyl (2S,3S)-2-(4-methoxyphenylamino)-3-methyl-4-oxo-hexanoate

ethyl (2S,3R)-2-(p-methoxyphenylamino)-3-methyl-4-oxohexanoate