Réaction #93689

ord-516606992516484ba946ff4032f48a0b

Solvants

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    LavageThe reaction solution is washed with water
  2. 2
    Séchagedried over sodium sulfate
  3. 3
    Autreevaporated to dryness under vacuum
  4. 4
    workup.STIRRINGThe residue is stirred up with 310 ml of ethanol
  5. 5
    Filtrationfiltered
  6. 6
    LavageThe filter cake is washed with 175 ml of ethanol
  7. 7
    Autredried under vacuum

Mode opératoire

A solution of 169 g of 5,6β-epoxy-7β-hydroxy-15β,16β-methylene-3β-pivaloyloxy-5β-androstan-17-one in a mixture of respectively 340 ml of dichloromethane, tetrachloromethane, and pyridine is combined with 200 g of triphenylphosphine and stirred for 2 hours at room temperature. The reaction solution is washed with water, dried over sodium sulfate, and evaporated to dryness under vacuum. The residue is stirred up with 310 ml of ethanol and filtered. The filter cake is washed with 175 ml of ethanol and dried under vacuum, thus obtaining 139.2 g of 7α-chloro-5,6β-epoxy-15β,16β-methylene-3β-pivaloyloxy-5β-androstan-17-one. An analytical sample, recrystallized from acetone-hexane, has a melting point of 228° C. [α]D =-100° (chloroform).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US04614616uspto-grants-1986_09