Réaction #1605828
ord-4b75e3c6798d4d5193b745c486679475
Équation de réaction
Réactifs
Aucun
Solvants
Conditions de réaction
Température
80°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-(Hydroxyethyl)phenol (2.7 g, 20.0 mmol) was dissolved in N,N-dimethylformamide (50 mL) and thereto were added potassium carbonate (6.90 g, 50.0 mmol) and 1,2-dibromoethane (15.03 g, 80.0 mmol). After stirring at 80° C. for 6 hours, the reaction solution was extracted with ethyl acetate. 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 2-[4-(2-bromoethoxy)phenyl]-1-ethanol (750.0 mg).