Reaktion #72988

ord-4b1946af6a0c4b97b5e7d559431d4d52

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Einengenwas concentrated under reduced pressure to a brown oil that
  2. 2
    Sonstigewas partitioned between water (100 mL) and dichloromethane (100 mL)
  3. 3
    ExtraktionThe aqueous layer was extracted with dichloromethane (3×100 mL)
  4. 4
    Trocknendried over Na2SO4
  5. 5
    Filtrationfiltered
  6. 6
    Einengenconcentrated to a light brown oil
  7. 7
    SonstigePurification by flash chromatography (silica gel, 40% ethyl acetate/hexanes)

Vorschrift

To a solution of 1,4-cyclohexanedione mono-ethylene ketal (30.0 g, 192 mmol) and nitromethane (15.6 mL, 288 mmol) in ethanol (18 mL) was added a solution of sodium ethoxide in ethanol (2.67 M, 3.4 mL, 9.6 mmol). The solution was stirred at room temperature (rt) for 5 days (d), then was concentrated under reduced pressure to a brown oil that was partitioned between water (100 mL) and dichloromethane (100 mL). The aqueous layer was extracted with dichloromethane (3×100 mL). The organic layers were combined, dried over Na2SO4, filtered, and concentrated to a light brown oil. Purification by flash chromatography (silica gel, 40% ethyl acetate/hexanes) provided the product 8-(nitromethyl)-1,4-dioxaspiro[4.5]decan-8-ol as a clear oil (16.7 g, 40%) that slowly formed clear crystals overnight.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08541438B2uspto-grants-2013_09