Reaktion #926934
ord-311258b4d8b04c22ae5ff05f3a7ec3ae
Reaktionsgleichung
Edukte
Reagenzien
Reaktionsbedingungen
Aufarbeitung
- 1Sonstigeequipped with a 5 inch Vigreaux column
- 2workup.DISTILLATIONdistillation
- 3TemperaturAfter heating at 120° for 16 hrs
- 4workup.DISTILLATION5 ml of distillate is collected
- 5TemperaturThe temperature is increased to 140° and after 45 mins an additional 60 ml of isopropenyl acetate
- 6Sonstigeis collected
- 7workup.ADDITIONThe residue is poured into 750 ml of ether
- 8Extraktionthe ether solution is extracted with saturated NaHCO3 solution and H2O
- 9ExtraktionThe ether extract
- 10Trocknenis dried over MgSO4
- 11Sonstigeevaporated in vacuo
- 12Sonstigeto give a residue
- 13Sonstigerecovered
- 14SonstigeThe residue is chromatographed on 300 g of neutral silica gel
- 15Waschenthe column is eluted with 0.5% acetone
Vorschrift
A solution of 1-acetoxy-3-methoxyestra-1,3,5(10)-trien-17-one (8.84 g, 26 mM), isopropenyl acetate (132 g, 1320 mM) and p-toluenesulfonic acid monohydrate (1.34 g, 7 mM) is heated at 120° in a distilling flask equipped with a 5 inch Vigreaux column to insure slow distillation. After heating at 120° for 16 hrs, 5 ml of distillate is collected. The temperature is increased to 140° and after 45 mins an additional 60 ml of isopropenyl acetate is collected. The residue is poured into 750 ml of ether and the ether solution is extracted with saturated NaHCO3 solution and H2O. The ether extract is dried over MgSO4 and evaporated in vacuo to give a residue containing the enol acetate and recovered starting material as the major components. The residue is chromatographed on 300 g of neutral silica gel and the column is eluted with 0.5% acetone:petroleum ether to give 1,17-diacetoxy-3 -methoxyestra-1,3,5(10),16-tetraene, yield 6.1 g (61%); m.p. 118° (petroleum ether).