Reaktion #8287

ord-0a2ba70e58064169870e248f2da8307c

Reaktionsgleichung

O=C(CO)c1ccccc1
2-hydroxyaceto-phenone
c1ccncc1
pyridine
CC(=O)OC(C)=O
acetic anhydride
CC(=O)OCC(=O)c1ccccc1
title compound
CC(=O)OCC(=O)c1ccccc1
Acetic Acid 2-oxo-2-phenyl-ethyl ester

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    WaschenThe mixture is washed with water (200 mL) and brine (200 mL)
  2. 2
    Trocknenthen dried over sodium sulfate
  3. 3
    FiltrationThe mixture is filtered
  4. 4
    Einengenconcentrated in vacuo

Vorschrift

A solution of 2-hydroxyaceto-phenone (10 g, 73.4 mmol), pyridine (17.4 g, 220.2 mmol), dichloromethane (734 mL), 3 crystals of 4-dimethylaminopyridine is cooled to −78° C. To this solution is added acetic anhydride (13.9 mL, 146.9 mmol) then warmed to room temperature and stirred for 18 h. The mixture is washed with water (200 mL) and brine (200 mL) then dried over sodium sulfate. The mixture is filtered and concentrated in vacuo to yield the title compound, 13 g (99%), as a colorless liquid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07087626B2uspto-grants-2006_08