Reaktion #1790641

ord-9c9e407c33794b408d3274b85d87cc29

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturto reflux for 15 minutes
  2. 2
    TemperaturThe solution was then cooled to 0°
  3. 3
    Sonstigewas partitioned between 1N HCl and methylene chloride
  4. 4
    ExtraktionThe aqueous phase was further extracted with methylene chloride
  5. 5
    Trocknendried over sodium sulfate
  6. 6
    Sonstigeevaporated

Vorschrift

To 40 ml of absolute ethanol was added 1.38 g (0.060 gram atom) metallic sodium. When the reaction was completed, 10.2 g (0.060 mole) of 3-acetylmercaptocycloheptene in 20 ml of absolute ethanol was added and the reaction mixture was brought up to reflux for 15 minutes. The solution was then cooled to 0° and 7.98 g (0.060 mole) of 1-nitro-2-acetoxyethane in 20 ml absolute ethanol was added. The reaction was allowed to proceed for 3.0 hours at 0° and then was partitioned between 1N HCl and methylene chloride. The aqueous phase was further extracted with methylene chloride. The organic phases were pooled, dried over sodium sulfate, and evaporated to afford 12 g (99%) of pure 3-[2-nitroethylthio]cycloheptene as a colorless oil.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04124595uspto-grants-1978_11