2-[Formyl(phenyl)amino]ethyl formate

Base Information

• Chemical Name: 2-[Formyl(phenyl)amino]ethyl formate
• CAS No.: 13238-43-2
• Molecular Formula: C₁₀H₁₁NO₃
• Molecular Weight: 193.202
• DSSTox Substance ID: DTXSID70698312
• Nikkaji Number: J3.109.310D
• Wikidata: Q82628488

Synonyms:SCHEMBL11194121;DTXSID70698312;2-[Formyl(phenyl)amino]ethyl formate;13238-43-2;Formic acid 2-(N-formylanilino)ethyl ester

Chemical Property of 2-[Formyl(phenyl)amino]ethyl formate

Chemical Property:

• XLogP3: 1.2
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 5
• Exact Mass: 193.07389321
• Heavy Atom Count: 14
• Complexity: 178

Purity/Quality:

85.0-99.8% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

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

Technology Process of 2-[Formyl(phenyl)amino]ethyl formate

There total 4 articles about 2-[Formyl(phenyl)amino]ethyl formate 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: 95.0%

4-Phenylmorpholine (92-53-5) → 2-(N-phenylformamido)ethyl formate (13238-43-2,6946-98-1)

Guidance literature:

With oxygen; In acetonitrile; at 20 ℃; for 48h; Wavelength; Solvent; Mechanism; UV-irradiation; Green chemistry;

DOI:10.1039/d1gc00743b

Reference yield: 46.0%

4-Phenylmorpholine (92-53-5) → 4-phenylmorpholin-3-one (29518-11-4) + 2-(N-phenylformamido)ethyl formate (13238-43-2,6946-98-1)

Guidance literature:

With ozone; In acetonitrile; at 25 ℃; for 24h; Solvent; Temperature; regioselective reaction; Mechanism;

DOI:10.1016/j.tet.2012.07.055

Reference yield:

4-Phenylmorpholine (92-53-5) → 2-(N-phenylformamido)ethyl formate (13238-43-2,6946-98-1) + C10H11NO

Guidance literature:

With 2,6-dimethylpyridine; (4s,6s)-2,4,5,6-tetra(9H-carbazol-9-yl)isophthalonitrile; oxygen; In acetonitrile; at 20 ℃; for 11h; Irradiation;

DOI:10.1002/adsc.202100455

upstream raw materials:

4-Phenylmorpholine

Downstream raw materials:

2-Anilinoethanol

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