1859-97-8

Basic information

• Product Name: Ethanone, 1-[2-(ethylamino)phenyl]-
• Synonyms: N-Aethyl-o-amino-acetophenon;1-(2-Aethylamino-phenyl)-aethanon;2-Aethylamino-acetophenon;1-(2-ethylamino-phenyl)-ethanone;N-Ethyl-2-acetylaniline
• CAS NO: 1859-97-8
• Molecular Formula: C10H13NO
• Molecular Weight: 163.219
• Mol File: 1859-97-8.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Ethanone, 1-[2-(ethylamino)phenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Ethanone, 1-[2-(ethylamino)phenyl]-(1859-97-8)
• EPA Substance Registry System: Ethanone, 1-[2-(ethylamino)phenyl]-(1859-97-8)

Safety Data

• Hazardous Substances Data: 1859-97-8(Hazardous Substances Data)

Upstream product

• 74-96-4 ethyl bromide 
• 551-93-9 2-aminoacetophenone 
• 75-03-6 ethyl iodide 
• 118-93-4 o-hydroxyacetophenone 
• 75-04-7 ethylamine 

Downstream Products

• 861803-79-4 1-ethyl-3-methyl-1H-indazole 
• 127286-32-2 1-ethyl-2-(2-thienyl)-4(1H)-quinolone 
• 528856-11-3 N-(2-acetylphenyl)-2,2,2-trichloro-N-ethylacetamide 

Relevant articles and documents

A process for the preparation method of the compound aromatic amines (by machine translation)

The invention discloses a method for preparing aromatic amine compounds, comprising the following steps: under protection of inert gas, with the ratio of the phenolic compound amine according to mole 1:2 - 40 are mixed and dissolved in the solvent, 50 - 140 °C reaction 6 - 15 hours, corresponding to preparing polymerizable aromatic amine compound, and then after treatment to obtain a pure aromatic amine compound. Raw materials of this invention generally are easy, simple operation, substrate and wide range of application, in the absence of catalyst under catalytic conditions of the phenolic compound can be obtained by nucleophilic addition reaction of the corresponding aromatic amine compound, and is suitable for industrial production. The present invention allows the presence of water in the reaction system, can be ammonia or hydrazine hydrate as the substrate, in order to ammonium chloride as a catalyst and a cosolvent, the success of the preparation to obtain a level from phenol hydroxy aromatic primary amino compound. The invention to phenol hydroxy has better selectivity, even if the presence of halogen atoms in the substrate does not affect the occurrence of the reaction. (by machine translation)

Selenium-promoted intramolecular oxidative amidation of 2-(arylamino)acetophenones for the synthesis of N-arylisatins

A convenient method for the synthesis of N-arylisatins from 2-(arylamino)acetophenones by using SeO2 as an oxidant is described. Various substituted N-arylisatins were selectively obtained in good to excellent yields. The reaction tolerates a wide range of functionalities. Copyright

Electrosynthesis of 3-chloro-1,4-disubstituted-2(1H)-quinolinones and 3,3-dichloro-4-hydroxy-1,4-disubstituted-3,4-dihydro-2(1H)-quinolinones, as well as a new convenient process to dioxindoles

Cathodic reduction of N-(2-acyl(or aroyl)phenyl)-2,2,2,-trichloro-N-alkylacetamide at - 1.2 V (vs SCE) under aprotic conditions yields 3-chloro-1,4-disubstituted-2(1H)-quinolinones (1) as the major product. When the reaction is carried out at -0.8 V (vs S