Реакция #1339
ord-cfae32b2602f43d987a2a67d53a3bee8
Уравнение реакции
Реактанты
Реагенты
Растворители
Условия реакции
Обработка
- 1Температураby external cooling under a nitrogen atmosphere
- 2Температураexternal cooling
- 3Другоеwas removed
- 4Другоеthe reaction quenched by the dropwise addition of saturated aqueous ammonium chloride solution
- 5ДругоеThe mixture was then partitioned between water and diisopropyl ether
- 6Другоеthe aqueous phase separated
- 7Промывкаwashed with diisopropyl ether (3×25 ml)
- 8ПромывкаThe organic phase was washed with brine
- 9Сушкаdried over anhydrous sodium sulphate
- 10Концентрированиеconcentrated by evaporation under reduced pressure
- 11ДругоеAfter purification by a procedure similar to
Методика
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.