Réaction #93689
ord-516606992516484ba946ff4032f48a0b
Équation de réaction
Réactifs
Réactifs
Solvants
Conditions de réaction
Traitement
- 1LavageThe reaction solution is washed with water
- 2Séchagedried over sodium sulfate
- 3Autreevaporated to dryness under vacuum
- 4workup.STIRRINGThe residue is stirred up with 310 ml of ethanol
- 5Filtrationfiltered
- 6LavageThe filter cake is washed with 175 ml of ethanol
- 7Autredried 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).