Reacción #64141
ord-004d54879f88431ca2eb482dd4019232
Ecuación de reacción
Reactantes
Reactivos
Ninguno
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1OtroAfter completion of the reaction
- 2TemperaturaThe reaction mixture was cooled
- 3Extracciónfollowed by extraction with chloroform
- 4SecadoSubsequently, the extract was dried over anhydrous sodium sulfate
- 5workup.DISTILLATIONChloroform and the remained ethyl α-bromoisobutyrate was distilled off under reduced pressure
Procedimiento
801 mg of {1-(4-bromobenzoyl)-4-(2-hydroxyphenyl)-4-hydroxypiperidine was stirred for 9 hours at the ambient temperature of 100° C. in the presence of 1.20 g (8.68 mmol) of potassium carbonate in 4.00 g (20.5 ml) of ethylα-bromoisobutyrate. After completion of the reaction, The reaction mixture was cooled, and water was added thereto, followed by extraction with chloroform. Subsequently, the extract was dried over anhydrous sodium sulfate. Chloroform and the remained ethyl α-bromoisobutyrate was distilled off under reduced pressure to obtain 902 mg (86.4%) of ethyl 3-{1-(4-bromobenzoyl)-4-hydroxypiperidin-4-yl}α,α-dimethylphenoxyacetate.