Reaktion #1339
ord-cfae32b2602f43d987a2a67d53a3bee8
Reaktionsgleichung
Edukte
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1Temperaturby external cooling under a nitrogen atmosphere
- 2Temperaturexternal cooling
- 3Sonstigewas removed
- 4Sonstigethe reaction quenched by the dropwise addition of saturated aqueous ammonium chloride solution
- 5SonstigeThe mixture was then partitioned between water and diisopropyl ether
- 6Sonstigethe aqueous phase separated
- 7Waschenwashed with diisopropyl ether (3×25 ml)
- 8WaschenThe organic phase was washed with brine
- 9Trocknendried over anhydrous sodium sulphate
- 10Einengenconcentrated by evaporation under reduced pressure
- 11SonstigeAfter purification by a procedure similar to
Vorschrift
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.