Reaktion #155319

ord-999ed3c345a447ad8033f1b12b11238b

Reaktionsgleichung

Cc1cc(N)c2occc2c1
5-Methylbenzofuran-7-ylamine
CCO
ethanol
Cc1cc(N)c2c(c1)CCO2
5-methyl-2,3-dihydrobenzofuran-7-ylamine
Ausbeute 87.6%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigefollowed by conduction of catalytic reduction at room temperature under ordinary pressure
  2. 2
    SonstigeThe catalyst was removed by celite filtration
  3. 3
    Sonstigecondensed under reduced pressure
  4. 4
    Trocknendried over anhydrous magnesium sulfate
  5. 5
    Einengenconcentrated to dryness under reduced pressure

Vorschrift

5-Methylbenzofuran-7-ylamine (1.3 g, 8.8 mmol) and 10% palladium carbon (500 mg) were added to ethanol (50 ml), followed by conduction of catalytic reduction at room temperature under ordinary pressure. The catalyst was removed by celite filtration, and the obtained filtrate was condensed under reduced pressure. The residue was dissolved in dichloromethane, dried over anhydrous magnesium sulfate, and then concentrated to dryness under reduced pressure, giving a white powder of 5-methyl-2,3-dihydrobenzofuran-7-ylamine (1.15 g, yield: 87%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: USRE045108E1uspto-grants-2014_09