Reaktion #1022

ord-c11fa99e3841426fba61a399ec0730d1

Reaktionsgleichung

O
water
CC(N)CO
2-amino-1-propanol
[H-].[Na+]
sodium hydride
N#Cc1ccc(Br)cc1
4-bromobenzonitrile
CC(N)COc1ccc(C#N)cc1
desired product
Ausbeute 41.0%
CC(N)COc1ccc(C#N)cc1
2-(4-cyanophenoxy)-1-methylethylamine
Ausbeute 41.0%

Reaktionsbedingungen

Temperatur
0°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONwas added dropwise to the reaction mixture
  2. 2
    SonstigeAfter completion of the reaction
  3. 3
    Extraktionextracted with ethyl acetate
  4. 4
    WaschenThe organic layer was washed with water
  5. 5
    Trocknendried over anhydrous magnesium sulfate
  6. 6
    SonstigeThe ethyl acetate was removed under reduced pressure
  7. 7
    workup.DISTILLATIONThe residue was distilled under reduced pressure

Vorschrift

50.0 g of 2-amino-1-propanol was added dropwise to a stirred mixture of 29.3 g of 60% sodium hydride and 300 mL of dimethylformamide at 0° C. After the reaction mixture was stirred for 30 minutes at 0° C. a solution containing 121.2 g of 4-bromobenzonitrile dissolved in N,N-dimethylformamide was added dropwise to the reaction mixture. The resultant mixture was stirred for 20 hours at room temperature. After completion of the reaction, the resultant mixture was poured into water and extracted with ethyl acetate. The organic layer was washed with water and then dried over anhydrous magnesium sulfate. The ethyl acetate was removed under reduced pressure. The residue was distilled under reduced pressure to obtain 48.0 g of the desired product (yield 41%). Boiling point: 132° C./0.26 mmHg.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05723469uspto-grants-1998_03