Reaktion #7970

ord-d0bd1b0c03f844d7a23d87971c34bc62

Reaktionsgleichung

[Cl-].[NH4+]
NH4Cl
COc1ccc2c(c1)C=CC2
5-methoxy-1H-indene
[Li][CH3]
MeLi
CCCI
iodopropane
CCCC1C=Cc2cc(OC)ccc21
5-methoxy-1-propyl-1H-indene
Ausbeute 108.3%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONadded dropwise over 10 minutes
  2. 2
    Temperaturcooled in an ice bath
  3. 3
    workup.STIRRINGThe mixture was stirred at ice bath temperature
  4. 4
    Temperaturwith gradual warming to room temperature
  5. 5
    workup.STIRRINGAfter stirring at room temperature overnight
  6. 6
    workup.STIRRINGshaken
  7. 7
    WaschenThe organic phase was washed with brine
  8. 8
    Trocknendried over MgSO4
  9. 9
    Filtrationfiltered
  10. 10
    Sonstigeevaporated under vacuum

Vorschrift

A solution of 5-methoxy-1H-indene (0.895 g, 6.12 mmol) in anhydrous Et2O (7.5 mL) was treated with 1.4M MeLi in Et2O (4.7 mL, 6.58 mmol) added dropwise over 10 minutes. The resulting hazy solution was stirred at room temperature an additional 15 minutes, then cooled in an ice bath and treated with iodopropane (1.00 mL, 10.3 mmol). The mixture was stirred at ice bath temperature with gradual warming to room temperature. After stirring at room temperature overnight, the mixture was treated with saturated aq. NH4Cl (10 mL) and Et2O (15 mL) and shaken. The organic phase was washed with brine, dried over MgSO4, filtered, and evaporated under vacuum to afford a mixture (1.248 g) of 5-methoxy-1-propyl-1H-indene and 6-methoxy-1-propyl-1H-indene as an oil.

Quelle

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