Réaction #1605808
ord-2d5d67bb480c4fef962afd9b4585a3a6
Équation de réaction
4-Hydroxypiperidine
potassium carbonate
(2-bromoethoxy)benzene
→
1-(2-phenoxyethyl)piperidin-4-ol
Rendement 76.6%
Réactifs
Aucun
Solvants
Conditions de réaction
Température
70°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.
Traitement
- 1ExtractionThe reaction solution was extracted with ethyl acetate
- 2Lavagethe organic layer was washed with a saturated aqueous solution of sodium chloride
- 3Séchagedried over anhydrous magnesium sulfate
- 4Concentrationconcentrated under reduced pressure
- 5AutreThe residue was purified by flash column chromatography
Mode opératoire
4-Hydroxypiperidine (5.06 g, 50 mmol) was dissolved in N,N-dimethylformamide (200 mL), potassium carbonate (13.8 g, 100 mmol) and (2-bromoethoxy)benzene (12.9 g, 60 mmol) were added thereto, and the mixture was stirred at 70° C. for 18 hours. The reaction solution was extracted with ethyl acetate and the organic layer was washed with a saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by flash column chromatography to obtain 1-(2-phenoxyethyl)piperidin-4-ol (8.48 g).