Reacción #3108
ord-e8deb101489c4e02b8ab82ed05f8e3e0
Ecuación de reacción
Reactantes
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1Temperaturaby external cooling under a nitrogen atmosphere
- 2Temperaturaexternal cooling
- 3Otrowas removed
- 4Otrothe reaction quenched by the dropwise addition of saturated aqueous ammonium chloride solution
- 5OtroThe mixture was then partitioned between water and diisopropyl ether
- 6Otrothe aqueous phase separated
- 7Lavadowashed with diisopropyl ether (3×25 ml)
- 8LavadoThe organic phase was washed with brine
- 9Secadodried over anhydrous sodium sulphate
- 10Concentraciónconcentrated by evaporation under reduced pressure
- 11OtroAfter purification by a procedure similar to
Procedimiento
Sodium t-butoxide (1.39 g of a 42% solution in dry dimethyl formamide was added dropwise over a period of 5 minutes to a stirred mixture of 1-bromo-1-chloro-2,2,2-trifluoroethane (0.535 ml), 3-methylbut-1-en-1-al (0.538 ml) and dry tetrahydrofuran (10 ml) maintained at a temperature of -78° C. by external cooling under a nitrogen atmosphere. The mixture was then stirred for a further 40 minutes at the temperature after which the external cooling was removed and the reaction quenched by the dropwise addition of saturated aqueous ammonium chloride solution. The mixture was then partitioned between water and diisopropyl ether and the aqueous phase separated, washed with diisopropyl ether (3×25 ml), and the washings combined with the organic phase. The organic phase was washed with brine and dried over anhydrous sodium sulphate and concentrated by evaporation under reduced pressure. After purification by a procedure similar to that set out in the previous Example there was obtained 5-bromo-5-chloro-4-hydroxy-2-methyl-6,6,6-trifluorohex-2-ene (1.39 g), identified by nuclear magnetic resonance and infra-red spectroscopy.