Reaction #476407

ord-fc2654983c52434986fb0f4c03a16532

Reaction equation

[Cl-].[K+]
potassium chloride
CC(=O)[O-].[K+]
potassium acetate
CC(=O)O
acetic acid
O=C(CCl)c1ccccc1
2-chloroacetophenone
CC(=O)OCC(=O)c1ccccc1
2-acetoxyacetophenone
Yield 79.3%

Solvents

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Workup

  1. 1
    TemperatureAfter completion of heating
  2. 2
    Filtrationwas filtered off
  3. 3
    workup.DISTILLATIONthe ethanol was distilled off in vacuo
  4. 4
    Otherto obtain a pale brown oily material
  5. 5
    Filtrationa precipitated solid was collected by filtration
  6. 6
    Otherrecrystallized from methanol

Procedure

78.5 g (0.80 mol) of potassium acetate, 5.0 g (0.08 mol) of acetic acid, and 123.7 g (0.80 mol) of 2-chloroacetophenone were heated under reflux in 500 mL of ethanol for 6 hours. After completion of heating, the reaction mixture was cooled to room temperature, deposited potassium chloride was filtered off, and the ethanol was distilled off in vacuo to obtain a pale brown oily material. This oily material was poured into one litter of water, and a precipitated solid was collected by filtration and recrystallized from methanol to obtain 113.1 g (yield: 79.3%) of 2-acetoxyacetophenone as a pale yellow solid.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08378116B2uspto-grants-2013_02