Реакция #73048
ord-a8faff76167a49a6a932dbb483511e5f
Уравнение реакции
Реагенты
Растворители
Условия реакции
Обработка
- 1Концентрированиеconcentrated under reduced pressure
- 2ДругоеThe residue was partitioned between chloroform (400 mL) and water (60 mL)
- 3ЭкстракцияThe aqueous was extracted with chloroform (5×100 mL)
- 4СушкаThe combined organics were dried over magnesium sulfate
- 5Фильтрацияfiltered
- 6Концентрированиеconcentrated under reduced pressure
- 7ДругоеThe residue was purified by HPFC
- 8Промывкаeluting with a gradient of 3-35% ethyl acetate in hexanes
Методика
Under a nitrogen atmosphere sodium methoxide (1.03 mL of 25 wt % in methanol, 4.51 mmol) was added dropwise to a solution of tetrahydro-4H-thiopyran-4-one (10.48 g, 90.20 mol) and nitromethane (7.33 mL, 135.3 mmol) in ethanol (6 mL). The reaction mixture was stirred at ambient temperature for 5 days and then concentrated under reduced pressure. The residue was partitioned between chloroform (400 mL) and water (60 mL). The aqueous was extracted with chloroform (5×100 mL). The combined organics were dried over magnesium sulfate, filtered, and then concentrated under reduced pressure. The residue was purified by HPFC eluting with a gradient of 3-35% ethyl acetate in hexanes to provide 10.23 g of 4-(nitromethyl)tetrahydro-2H-thiopyran-4-ol.