Reacción #56620

Ecuación de reacción

3,7β-dihydroxy-2-iodo-estra-1,3,5(10)-trien-17-one

aluminum isopropylate

→

colorless crystals

Rendimiento 63.0%

3-Hydroxy-2-iodo-estra-1,3,5(10)-triene-7,17-dione

Rendimiento 63.0%

Disolventes

toluene

cyclohexanone

toluene

Condiciones de reacción

Tratamiento posterior

1. 1
   workup.DISTILLATIONIn the meantime, a portion of the reaction mixture was distilled off
2. 2
   workup.ADDITIONAfter complete addition of the aluminum isopropylate, it
3. 3
   Temperaturawas refluxed for still another 5 hours
4. 4
   TemperaturaThen, the reaction solution was cooled
5. 5
   workup.ADDITIONdiluted with 80 ml of dichloromethane and 30 ml of potassium/sodium tartrate solution
6. 6
   Otrowas separated from the aqueous phase
7. 7
   ExtracciónThe aqueous phase was finally extracted with dichloromethane (3×30 ml)
8. 8
   Lavadothe combined organic phases were washed with a saturated NaCl solution
9. 9
   Otrodried on sodium sulfate
10. 10
    Concentraciónconcentrated by evaporation in a rotary evaporator

Procedimiento

A solution of 206 mg (0.5 mmol) of 3,7β-dihydroxy-2-iodo-estra-1,3,5(10)-trien-17-one 14 in 15 ml of toluene and 4 ml of cyclohexanone was heated to 140° C. (oil bath temperature), and a solution of 400 mg of aluminum isopropylate in 10 ml of toluene was added drop by drop. In the meantime, a portion of the reaction mixture was distilled off. After complete addition of the aluminum isopropylate, it was refluxed for still another 5 hours. Then, the reaction solution was cooled and diluted with 80 ml of dichloromethane and 30 ml of potassium/sodium tartrate solution, and the resulting mixture was first stirred vigorously for 30 minutes before the organic phase was separated from the aqueous phase. The aqueous phase was finally extracted with dichloromethane (3×30 ml), and the combined organic phases were washed with a saturated NaCl solution, dried on sodium sulfate and concentrated by evaporation in a rotary evaporator. Flash chromatography (cyclohexane/ethyl acetate) yielded 129 mg (63%) of colorless crystals.

Fuente