Reaktion #1605811

ord-ff96e38209dc4889b9b2b3a22262ad75

Reaktionsgleichung

Nc1ccccc1-c1ccccc1
2-Phenylaniline
CC(=O)OC(C)=O
acetic anhydride
CC(=O)Nc1ccccc1-c1ccccc1
2-phenyl-N-acetylaniline
Ausbeute 99.5%

Reagenzien

Keine

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    EinengenThe solution was concentrated under reduced pressure
  2. 2
    workup.ADDITIONto the residue was added water (15 mL)
  3. 3
    workup.STIRRINGthe mixture was stirred at room temperature for 3 hours
  4. 4
    FiltrationThe precipitate was collected by filtration
  5. 5
    Waschenwashed with purified water
  6. 6
    Sonstigedried under reduced pressure

Vorschrift

2-Phenylaniline (5 g, 29.55 mmol) was dissolved in acetic acid (30 mL), acetic anhydride (3.62 g, 35.45 mmol) was added thereto under ice bath, and the mixture was stirred under ice bath for 2 hours. The solution was concentrated under reduced pressure. to the residue was added water (15 mL), and the mixture was stirred at room temperature for 3 hours. The precipitate was collected by filtration, washed with purified water, and dried under reduced pressure to obtain 2-phenyl-N-acetylaniline (6.21 g).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09072734B2uspto-grants-2015_07