Réaction #417964

ord-b36c980b138d4933833e7cd7a8fdd153

Équation de réaction

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
Rendement 93.0%
CC(=O)Nc1ccc(Cl)c(O)c1
N-(4-chloro-3-hydroxyphenyl)acetamide
Rendement 93.0%

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températurethe reaction was refluxed for 5 mins
  2. 2
    FiltrationIt was filtered off
  3. 3
    Lavagewashed with water (10 mL)
  4. 4
    Autredried

Mode opératoire

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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US08877752B2uspto-grants-2014_11