Reaktion #168163

ord-abbecd99663840539e4f37761a82b03f

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturthe mixture was refluxed for 10 h
  2. 2
    FiltrationThe solution was filtered
  3. 3
    Einengenthe filtrate was concentrated
  4. 4
    Sonstigeto afford the crude product, which
  5. 5
    Sonstigewas purified by column chromatography

Vorschrift

To a solution of methanesulfonic acid 2-(2-isopropyl-[1,3]dioxolan-2-yl)-ethyl ester (12 g, 50 mmol) and (S)-1-(4-bromophenyl)ethanamine (19.9 g, 100 mmol) in CH3CN (250 mL) was added K2CO3 (8 g, 58 mmol), and the mixture was refluxed for 10 h. The solution was filtered, and the filtrate was concentrated to afford the crude product, which was purified by column chromatography to give [(S)-1-(4-bromophenyl)-ethyl]-[2-(2-isopropyl-[1,3]dioxolan-2-yl)-ethyl]-amine (6.5 g, 38%).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08846668B2uspto-grants-2014_09