Toluene → HCID 86740367, Verbindung

HRID 464153Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 464153
C([C@@]12[C@@H:20]3[C@H:11]([C@H:12]4[C@@:16]([CH2:18][CH2:19]3)([CH3:17])[C:15](=[O:21])[CH2:14][CH2:13]4)[CH2:10][CH2:9]C1=CC(=O)CC2)C.[C:23]1(Cl)C(=O)C(Cl)=C(Cl)C(=O)[C:24]=1Cl.[C:35]1([CH3:41])[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=1>>[CH2:41]=[C:35]1[CH2:40][CH2:39][C@@:38]2([CH2:23][CH3:24])[C:37]([CH:9]=[CH:10][C@@H:11]3[C@@H:20]2[CH2:19][CH2:18][C@@:16]2([CH3:17])[C@H:12]3[CH2:13][CH2:14][C:15]2=[O:21])=[CH:36]1

Komponenten

4

Versuchsvorschrift

290 mg of 10β-ethyl-estra-4-ene-3,17-dione and 594 mg of chloranil are taken up in 15 ml of toluene. The mixture is refluxed for 20 hours in an atmosphere of nitrogen. The solvent is washed with several small portions of 5% sodium hydroxide and then with water. It is dried over anhydrous sodium sulfate for several hours. The solution is filtered and the solvent removed under vacuum. The amorphous solid obtained is triturated with ether, filtered and purified by chromatography over silica gel using a n-hexane-ethyl acetate solvent.

Aufarbeitung

  1. temperatureThe mixture is refluxed for 20 hours in an atmosphere of nitrogen
  2. washThe solvent is washed with several small portions of 5% sodium hydroxide
  3. dry with materialIt is dried over anhydrous sodium sulfate for several hours
  4. filtrationThe solution is filtered
  5. customthe solvent removed under vacuum
  6. customThe amorphous solid obtained
  7. customis triturated with ether
  8. filtrationfiltered
  9. custompurified by chromatography over silica gel using a n-hexane-ethyl acetate solvent

Quellen und Nachweise

ORD-Eintrag
ord-c5a9462c548345a4b9e29d8527ecbb80
Quelldatensatz
uspto-grants-1985_10
Patentnummer
US04546098

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