Реакция #2348469
ord-c93a3c5a5b41463ea504659dc142aa7c
Уравнение реакции
Реактанты
Реагенты
Растворители
Условия реакции
Обработка
- 1ТемператураThe reaction mixture was cooled to room temperature
- 2workup.STIRRINGThe mixture was stirred at room temperature for 18 hours
- 3Экстракцияthe reaction mixture was extracted with ethyl acetate
- 4ПромывкаThe extract was washed with aqueous saturated sodium chloride
- 5Сушкаdried over anhydrous sodium sulfate
- 6Концентрированиеconcentrated under reduced pressure
Методика
4.49 g of 2,2-dimethyl-6-(tetrahydro-2H-pyran-2-yloxy)-4-hexyn-3-one was dissolved in 20 ml of methanol, and 1.30 g of sodium methoxide and 1.53 g of hydroxylamine hydrochloride were added. The mixture was stirred at 70° C. for 2 hours. The reaction mixture was cooled to room temperature and then adjusted to pH 2 with concentrated hydrochloric acid. The mixture was stirred at room temperature for 18 hours. After aqueous saturated sodium hydrogen carbonate was added, the reaction mixture was extracted with ethyl acetate. The extract was washed with aqueous saturated sodium chloride, dried over anhydrous sodium sulfate and then concentrated under reduced pressure. The residue was subjected to silica gel column chromatography to obtain 1.12 g of (3-t-butyl-isoxazol-5-yl)methanol.