Reacción #1833223
ord-abcfd28db41d491a8c69383a55980740
Ecuación de reacción
Reactantes
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1TemperaturaAfter cooling
- 2Extracciónextracted three times with diethyl ether (80 mL portions)
- 3LavadoThe combined extracts were washed with water (15 mL), 2.0 M NaOH (45 mL)
- 4Secadodried (Na2SO4)
- 5Concentraciónconcentrated by rotary evaporation
- 6OtroThe material was purified by silica gel chromatography
- 7Lavadoeluting with hexane
Procedimiento
2-Bromo-6-fluorophenol (10.2 g, 53 mmol), potassium carbonate (7.3 g, 53 mmol), 1,2-dibromo-tetrafluoroethane (21 g, 80 mmol) and 1-butanethiol (1.1 g, 12 mmol) were combined in dry N,N-dimethylformamide (75 mL) and heated to 50° C. in a stirred pressure reactor. After cooling, the contents were mixed with 1.0 M sodium hydroxide (NaOH; 100 mL) and extracted three times with diethyl ether (80 mL portions). The combined extracts were washed with water (15 mL), 2.0 M NaOH (45 mL), dried (Na2SO4) and concentrated by rotary evaporation. The material was purified by silica gel chromatography eluting with hexane to afford the title compound as a clear liquid (15 g, 76%): 1H NMR (400 MHz, CDCl3) δ 7.48-7.39 (m, 1H), 7.22-7.14 (m, 2H); EIMS m/z 368.