Reacción #45002
ord-a4df0e5f14c14062970be199319756ce
Ecuación de reacción
Reactivos
Ninguno
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1TemperaturaThe reaction mixture was heated
- 2Temperaturaat reflux for 6 h
- 3Otrothe solvent was removed under vacuum
- 4ExtracciónThe residue was extracted with ethyl acetate (3×15 mL)
- 5Lavadothe combined organic layers were washed with saturated NaCl solution (10 mL)
- 6Secadodried over MgSO4
- 7Concentraciónconcentrated
Procedimiento
To a solution of 3-hydroxybenzylalcohol (2.4 g, 20 mmol) in THF (50 mL) and water (2.5 mL) was first added powdered sodium hydroxide (1.5 g, 37.5 mmol) and then a solution of propargyl bromide, dissolved as an 80% weight solution in xylene (3.36 mL, 30 mmol). The reaction mixture was heated at reflux for 6 h. To the mixture was added 10% citric acid (2.5 mL) and the solvent was removed under vacuum. The residue was extracted with ethyl acetate (3×15 mL) and the combined organic layers were washed with saturated NaCl solution (10 mL), dried over MgSO4 and concentrated to give the 3-propargyloxybenzyl alcohol.