Reaktion #417964

ord-b36c980b138d4933833e7cd7a8fdd153

Reaktionsgleichung

CC(=O)OC(C)=O
Acetic anhydride
Nc1ccc(Cl)c(O)c1
4-chloro-3-hydroxy aniline
CC(=O)Nc1ccc(Cl)c(O)c1
product 17a
Ausbeute 93.0%
CC(=O)Nc1ccc(Cl)c(O)c1
N-(4-chloro-3-hydroxyphenyl)acetamide
Ausbeute 93.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturthe reaction was refluxed for 5 mins
  2. 2
    FiltrationIt was filtered off
  3. 3
    Waschenwashed with water (10 mL)
  4. 4
    Sonstigedried

Vorschrift

Acetic anhydride (3.0 mL, 42.0 mmol) was added to a solution of 4-chloro-3-hydroxy aniline (4.0 g, 28 mmol) in acetic acid (20 mL), and the reaction was refluxed for 5 mins. The reaction mixture was cooled to room temperature and the product was solidified. It was filtered off and washed with water (10 mL) and dried to obtain the product 17a in 93% yield (4.8 g) as a creamy white solid. There was no need for further purification.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08877752B2uspto-grants-2014_11