Reaktion #7972

ord-3f65a22cc30c4c71b7a3d15e3263d86d

Reaktionsgleichung

CCCC1CCc2ccc(OC)cc21
indans
CCCC1CCc2ccc(OC)cc21
6-methoxy-1-propyl-indan
[K+].[O]=[Mn](=[O])(=[O])[O-]
KMnO4
CCCC1CC(=O)c2ccc(OC)cc21
5-methoxy-3-propyl-1-indanone
Ausbeute 15.1%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe resulting mixture was heated
  2. 2
    Temperaturat reflux for 89 hours
  3. 3
    Filtrationfiltered through a celite pad
  4. 4
    TrocknenThe filtrate was dried over MgSO4
  5. 5
    Filtrationfiltered
  6. 6
    Sonstigeevaporated under vacuum to an oil (1.155 g)
  7. 7
    SonstigeThe crude product was purified by chromatography on a Biotage FLASH 12M column
  8. 8
    Wascheneluting with 10% EtOAc in hexanes

Vorschrift

The mixture of indans from step 2 (1.287 g, approx. 6.1 mmol) in CH2Cl2 (50 mL) was treated with a finely ground mixture of KMnO4 (7.00 g) and CuSO4.xH2O. The resulting mixture was heated at reflux for 89 hours, then cooled to room temperature and filtered through a celite pad. The filtrate was dried over MgSO4, filtered and evaporated under vacuum to an oil (1.155 g). The crude product was purified by chromatography on a Biotage FLASH 12M column, eluting with 10% EtOAc in hexanes, to afford 5-methoxy-3-propyl-1-indanone (0.188 g) as an oil. Other column fractions afforded 6-methoxy-3-propyl-1-indanone, the indan starting materials, and 5-methoxy-1-indanone.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07087599B2uspto-grants-2006_08