Reaktion #54525

ord-10a7dcf0f1bc44019dfc64a79c0a83bc

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturIt was cooled
  2. 2
    Filtrationfiltered
  3. 3
    Waschenthe cake washed with ether
  4. 4
    SonstigeThe solvent was evaporated through a 9" Vigreux
  5. 5
    workup.DISTILLATIONthe product distilled at 91° (13 mm), 3.5 g

Vorschrift

A solution of the trans-N-[2-(N,N-dimethylamino)cyclohexyl]acetamide (acetyl compound) (5.03 g.; 0.027 mole) in 100 ml. of ether was added during 10 minutes to a solution of LAH (5.03 g.) in 300 ml. of ether and the mixture was refluxed 24 hours. It was cooled, decomposed in succession with 5 ml. of H2O, 5 ml. of 15% NaOH, and 15 ml. of H2O. The suspension was stirred 1 hour at room temperature, filtered and the cake washed with ether. The solvent was evaporated through a 9" Vigreux and the product distilled at 91° (13 mm), 3.5 g. (76% yield). ir NH3680 w, 3,300; CH 2960, 2920, 2850, 2820; N-alkyl 2780, CH/CN 1455, 1265, 1140, 1060, 1045, 1025, 1025. NMR in CDCl3 (100 MHz) was in accord. Mass spectrum M+ 170.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04148914uspto-grants-1979_04