Reaktion #1023

ord-6d97a1bfa8604b93849d4516305a87c9

Reaktionsgleichung

CC(N)CO
2-amino-1-propanol
[H-].[Na+]
sodium hydride
Cl.Clc1ccncc1
4-chloropyridine hydrochloride
CC(N)COc1ccncc1
desired product
Ausbeute 30.2%
CC(N)COc1ccncc1
1-methyl-2-(4-pyridyloxy)ethylamine
Ausbeute 30.2%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.STIRRINGThe mixture was stirred for 20 hours at room temperature
  2. 2
    SonstigeAfter completion of the reaction
  3. 3
    Filtrationthe solids were filtered off
  4. 4
    SonstigeThe solvent in the filtrate was removed under reduced pressure
  5. 5
    SonstigeThe residue was purified by column chromatography on silica gel

Vorschrift

6.2 g of 2-amino-1-propanol was added dropwise to a stirred mixture of 4.0 g of 60% sodium hydride and 50 mL of N,N-dimethylformamide at 5° C.-10° C. After the reaction mixture was stirred for 30 minutes, 12.5 g of 4-chloropyridine hydrochloride in limited amounts was added to the reaction mixture. The mixture was stirred for 20 hours at room temperature. After completion of the reaction, the solids were filtered off. The solvent in the filtrate was removed under reduced pressure. The residue was purified by column chromatography on silica gel to obtain 3.8 g of the desired product (yield: 30%). Refractive index: 1.5469.

Quelle

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