تفاعل #93001

ord-a7eafb5a9e0f40e9a62afd5c8aa56723

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONis added
  2. 2
    غسيلThe mixture is washed with 10% H3PO4, water, 10% aqueous NaHCO3, water and saturated aqueous sodium chloride solution in that order
  3. 3
    تجفيفdried over anhydrous magnesium sulfate
  4. 4
    workup.DISTILLATIONThe solvent is then distilled off
  5. 5
    غسيلpassage of 80 ml of diisopropyl ether-n-hexane (1:10), elution
  6. 6
    workup.ADDITIONis carried out with 80 ml of a 1:1 mixture of the same solvents
  7. 7
    أخرىThe eluate is evaporated under reduced pressure
  8. 8
    أخرىto remove the solvent

الإجراء التجريبي

In 10 ml of dichloromethane are dissolved 0.5 g of 16β-ethyl-17β-glycoloyloxy-4-estren-3-one and 0.2 ml of N,N-dimethylaniline and, with stirring, 0.3 ml of cyclopentylacetyl chloride is added. The mixture is stirred at room temperature (15°-25° C.) overnight and 150 ml of ethyl acetate is added. The mixture is washed with 10% H3PO4, water, 10% aqueous NaHCO3, water and saturated aqueous sodium chloride solution in that order and dried over anhydrous magnesium sulfate. The solvent is then distilled off and the residue is subjected to column chromatography. Following passage of 80 ml of diisopropyl ether-n-hexane (1:10), elution is carried out with 80 ml of a 1:1 mixture of the same solvents. The eluate is evaporated under reduced pressure to remove the solvent, giving 0.1 g of the above-identified compound as a colorless viscous oil.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04609650uspto-grants-1986_09