Reaktion #93684
ord-5863de6b20274167aa1ba7298b338112
Reaktionsgleichung
Edukte
Reagenzien
Reaktionsbedingungen
Aufarbeitung
- 1Temperaturheated to 41°-49° over a period of 6 hrs at which time TLC
- 2workup.ADDITIONCelite (5 g) is added
- 3workup.STIRRINGthe mixture stirred 1/2 hr at 20°-25°
- 4FiltrationThe mixture is filtered through Celite (5 g)
- 5Waschenthe solids washed with methanol/THF
- 6EinengenThe filtrate and washings are concentrated under reduced pressure to about 35 ml, at which point crystals
- 7Sonstigebegin forming
- 8Einengenthe mixture again concentrated under reduced pressure
- 9workup.WAITto sit overnight at 20°-25° under nitrogen atmosphere
- 10workup.ADDITIONWater (500 ml) is added
- 11workup.STIRRINGslowly at first, with stirring over a period of 15 min
- 12FiltrationThe mixture is filtered
- 13Waschenthe solids washed with water (3×20 ml), and hexane (2×10 ml)
- 14SonstigeThe solids were dried under nitrogen
Vorschrift
Mercuric oxide red (0.32 g) was mixed with sulfuric acid/water (sulfuric acid, 0.4 ml; water, 6.0 ml) and let stand overnight. 17α-Ethynyl-17β-hydroxy-6,16-dimethyleneandrosta-4-en-3-one (Example 4, 5.0 g) is mixed with THF (15 ml). The mercuric sulfate solution is added the reaction heated to 41°-49° over a period of 6 hrs at which time TLC indicates the reaction is completed. Sodium carbonate (0.79 g) in water (10 ml) is added and the mixture stirred for 5 min. Celite (5 g) is added and the mixture stirred 1/2 hr at 20°-25°. The mixture is filtered through Celite (5 g), the solids washed with methanol/THF; 1/1 (2×10 ml) and once with THF (10 ml), followed by methylene chloride (10 ml). The filtrate and washings are concentrated under reduced pressure to about 35 ml, at which point crystals begin forming. Methanol (50 ml) is added and the mixture again concentrated under reduced pressure and permitted to sit overnight at 20°-25° under nitrogen atmosphere. Water (500 ml) is added, slowly at first, with stirring over a period of 15 min. The mixture is filtered, the solids washed with water (3×20 ml), and hexane (2×10 ml). The solids were dried under nitrogen to give the title compound.