Reaction #3108
ord-e8deb101489c4e02b8ab82ed05f8e3e0
Reaction equation
Reactants
Reagents
Solvents
Conditions
Workup
- 1Temperatureby external cooling under a nitrogen atmosphere
- 2Temperatureexternal cooling
- 3Otherwas removed
- 4Otherthe reaction quenched by the dropwise addition of saturated aqueous ammonium chloride solution
- 5OtherThe mixture was then partitioned between water and diisopropyl ether
- 6Otherthe aqueous phase separated
- 7Washwashed with diisopropyl ether (3×25 ml)
- 8WashThe organic phase was washed with brine
- 9Dryingdried over anhydrous sodium sulphate
- 10Concentrationconcentrated by evaporation under reduced pressure
- 11OtherAfter purification by a procedure similar to
Procedure
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.