Reaktion #50340
ord-9f4906b82f104ab08ee7e55757ce1dce
Reaktionsgleichung
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1Sonstigedegassed
- 2workup.ADDITIONThis solution is added dropwise over 20 min to a freshly degassed slurry of chromic chloride hexahydrate (81 mg), thiovanic acid (0.70 ml) and zinc dust (555 mg) in DMF (4 ml) at 0° THF (about 8 ml)
- 3Waschenfor rinse purposes
- 4Temperaturis slowly heated to 50°
- 5SonstigeThe THF is removed by vacuum distillation
- 6workup.ADDITIONthe remaining slurry is diluted with ethyl acetate (25 ml) and water (25 ml)
- 7SonstigeThe unreacted zinc is removed by filtration
- 8Waschenis washed with aqueous ethyl acetate
- 9WaschenThe combined filtrate and wash
- 10Sonstigeto separate
- 11WaschenThe organic layer is washed with water (3×25 ml)
- 12Einengenfinally is concentrated under vacuum to a residue
- 13SonstigeThe residue is recrystallized from 1 part toluene and 2 parts heptane
Vorschrift
9α-Bromo-11β-hydroxyandrost-4-ene-3,17-dione (I, PREPARATION 2, 2.134 g) is dissolved in THF (THF 20ml) and degassed as described in EXAMPLE 1. This solution is added dropwise over 20 min to a freshly degassed slurry of chromic chloride hexahydrate (81 mg), thiovanic acid (0.70 ml) and zinc dust (555 mg) in DMF (4 ml) at 0° THF (about 8 ml) is used for rinse purposes. The slurry is stirred at 0° to 2° for 2.2 hr and then is slowly heated to 50°. The THF is removed by vacuum distillation and the remaining slurry is diluted with ethyl acetate (25 ml) and water (25 ml). The unreacted zinc is removed by filtration and is washed with aqueous ethyl acetate. The combined filtrate and wash is allowed to separate. The organic layer is washed with water (3×25 ml) and finally is concentrated under vacuum to a residue. The residue is recrystallized from 1 part toluene and 2 parts heptane to give the title compound, TLC Rf =0.45 (methanol/methylene chloride, 5/95); HPLC 96.7% (II), 2.9% ∆9(11).