Реакция #73048

ord-a8faff76167a49a6a932dbb483511e5f

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Концентрированиеconcentrated under reduced pressure
  2. 2
    ДругоеThe residue was partitioned between chloroform (400 mL) and water (60 mL)
  3. 3
    ЭкстракцияThe aqueous was extracted with chloroform (5×100 mL)
  4. 4
    СушкаThe combined organics were dried over magnesium sulfate
  5. 5
    Фильтрацияfiltered
  6. 6
    Концентрированиеconcentrated under reduced pressure
  7. 7
    ДругоеThe residue was purified by HPFC
  8. 8
    Промывкаeluting 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.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08541438B2uspto-grants-2013_09