p-Bromoacetophenone → 4-Bromophenacyl bromide

HRID 45652

Reaktionsgleichung

Reaktionsgleichung von HRID 45652
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8](=[O:10])[CH3:9])=[CH:4][CH:3]=1.[Br:11]Br>C(O)(=O)C>[Br:11][CH2:9][C:8]([C:5]1[CH:6]=[CH:7][C:2]([Br:1])=[CH:3][CH:4]=1)=[O:10]

Komponenten

4

Reaktionsbedingungen

Temperatur
60 °C

Versuchsvorschrift

Into a 250-mL 3-necked round-bottom flask, was placed a solution of 1-(4-bromophenyl)ethanone (10.0 g, 50.25 mmol, 1.00 equiv) in acetic acid (50 mL). This was followed by the addition of a solution of bromine (8.2 g, 1.05 equiv) in acetic acid (50 mL) dropwise with stirring at 60° C. over 90 min. The resulting solution was stirred for 3 h at 60° C. The resulting mixture was concentrated under vacuum. The crude product was re-crystallized from petroleum ether/ethyl acetate in the ratio of 7:1. This resulted in 9.3 g (67%) of the title compound as a yellow solid.

Aufarbeitung

  1. customInto a 250-mL 3-necked round-bottom flask, was placed
  2. stirringThe resulting solution was stirred for 3 h at 60° C
  3. concentrationThe resulting mixture was concentrated under vacuum
  4. customThe crude product was re-crystallized from petroleum ether/ethyl acetate in the ratio of 7:1

Quellen und Nachweise

ORD-Eintrag
ord-531419fd15e1467baf639234e50ceeb9
Quelldatensatz
uspto-grants-2013_09
Patentnummer
US08541448B2

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