Reacción #48045
ord-8cb30b2a5fa74259aa6b20b955ff6ebf
Ecuación de reacción
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Temperatura
0°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1Otroat 0° C
- 2Extracciónthe resulting mixture was extracted with DCM
- 3LavadoThe combined organic extracts were washed with brine
- 4Secadodried (MgSO4)
- 5Filtraciónfiltered
- 6Concentraciónconcentrated in vacuo
- 7Otroto give a residue which
- 8Otrowas purified by flash column chromatography (100% pentane)
Procedimiento
To a solution of 5.66 g of 1-(4-bromophenyl)-cyclobutanol (24.92 mmol, described in example S2-A) in 70 ml DCM were added 4.23 g of (diethylamino)sulfur trifluoride (95%, 24.92 mmol) at 0° C. The reaction mixture was stirred at 0° C. for 35 min, then sat. NaHCO3— solution was added and the resulting mixture was extracted with DCM. The combined organic extracts were washed with brine, dried (MgSO4), filtered, and concentrated in vacuo to give a residue which was purified by flash column chromatography (100% pentane) to give 1-bromo-4-(1-fluoro-cyclobutyl)-benzene (3.66 g, 64%) as a colorless liquid.