Reaktion #1519138

ord-3688ae2d4b5c49a88bc8b07903c5c041

Reaktionsgleichung

O=Cc1cc(Br)ccc1O
5-bromo-2-hydroxybenzaldehyde
O=C([O-])[O-].[K+].[K+]
potassium carbonate
C=CCCBr
4-bromobut-1-ene
CC(C)=O
acetone
C=CCCOc1ccc(Br)cc1C(O)CC(C)=O
4-[5-bromo-2-(but-3-en-1-yloxy)phenyl]-4-hydroxybutan-2-one

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturthe reaction mixture is then heated
  2. 2
    Temperaturat reflux for 36 hours
  3. 3
    Temperaturbefore being cooled
  4. 4
    Filtrationfiltered
  5. 5
    Sonstigeevaporated to dryness

Vorschrift

To 300 ml of acetone there are added 10 g of 5-bromo-2-hydroxybenzaldehyde (49.7 mmol), 13.7 g of potassium carbonate (99.5 mmol) and 10.1 ml of 4-bromobut-1-ene (99.5 mmol); the reaction mixture is then heated at reflux for 36 hours before being cooled, filtered and evaporated to dryness to yield 4-[5-bromo-2-(but-3-en-1-yloxy)phenyl]-4-hydroxybutan-2-one in the form of an oil.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07612061B2uspto-grants-2009_11