Reaction #50340
ord-9f4906b82f104ab08ee7e55757ce1dce
Reaction equation
Reagents
Solvents
Conditions
Workup
- 1Otherdegassed
- 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)
- 3Washfor rinse purposes
- 4Temperatureis slowly heated to 50°
- 5OtherThe THF is removed by vacuum distillation
- 6workup.ADDITIONthe remaining slurry is diluted with ethyl acetate (25 ml) and water (25 ml)
- 7OtherThe unreacted zinc is removed by filtration
- 8Washis washed with aqueous ethyl acetate
- 9WashThe combined filtrate and wash
- 10Otherto separate
- 11WashThe organic layer is washed with water (3×25 ml)
- 12Concentrationfinally is concentrated under vacuum to a residue
- 13OtherThe residue is recrystallized from 1 part toluene and 2 parts heptane
Procedure
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).