Reacción #5139

ord-8aee444aa73b42c2854984330a5ca68e

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroobtained in Reference Example 2
  2. 2
    workup.STIRRINGby stirring for further 4 hours
  3. 3
    Lavadothe mixture was washed with saturated aqueous sodium chloride solution
  4. 4
    SecadoAfter drying over anhydrous magnesium sulfate
  5. 5
    workup.DISTILLATIONthe solvent was distilled off under reduced pressure
  6. 6
    OtroThe obtained crude product
  7. 7
    Otrowas recrystallized from toluene

Procedimiento

In 400 ml of methylene chloride was suspended 40.0 g of Compound b obtained in Reference Example 2. Trifluoroacetic anhydride, 21.0 ml, was added to the suspension followed by stirring at room temperature for an hour. Them, 10.7 ml of 2-mercaptoethanol was added to the mixture followed by stirring for further 4 hours. After 100 ml of methylene chloride was added to the reaction mixture, the mixture was washed with saturated aqueous sodium chloride solution. After drying over anhydrous magnesium sulfate, the solvent was distilled off under reduced pressure. The obtained crude product was recrystallized from toluene to give 37.6 g of methyl 11-(2-hydroxyethyl)thio-6,11-dihydrodibenz[b,e]oxepin-2-carboxylate as white crystals.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05242931uspto-grants-1993_09