Réaction #1023
ord-6d97a1bfa8604b93849d4516305a87c9
Équation de réaction
2-amino-1-propanol
sodium hydride
4-chloropyridine hydrochloride
→
desired product
Rendement 30.2%
1-methyl-2-(4-pyridyloxy)ethylamine
Rendement 30.2%
Réactifs
Aucun
Solvants
Conditions de réaction
Conditions détaillées
See reaction.notes.procedure_details.
Traitement
- 1workup.STIRRINGThe mixture was stirred for 20 hours at room temperature
- 2AutreAfter completion of the reaction
- 3Filtrationthe solids were filtered off
- 4AutreThe solvent in the filtrate was removed under reduced pressure
- 5AutreThe residue was purified by column chromatography on silica gel
Mode opératoire
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.