Water → HCID 86736333, Verbindung

HRID 1390791Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1390791
CC(C)=O.OS(O)(=O)=O.O=[Cr](=O)=O.[C:14]([O:17][C@H:18]1[CH2:23][CH2:22][C@H:21]2[C@H:24]3[C@H:35]([CH2:36][CH2:37][C@:19]12[CH3:20])[C@:32]1([CH2:33][OH:34])[C:27]([CH2:28][C@@H:29]([O:38][CH2:39][CH3:40])[CH2:30][CH2:31]1)=[CH:26][CH2:25]3)(=[O:16])[CH3:15].O>CC(C)=O>[C:14]([OH:17])(=[O:16])[CH3:15].[CH2:39]([O:38][C@H:29]1[CH2:30][CH2:31][C@@:32]2([CH:33]=[O:34])[C:27](=[CH:26][CH2:25][C@@H:24]3[C@@H:35]2[CH2:36][CH2:37][C@@:19]2([CH3:20])[C@H:21]3[CH2:22][CH2:23][C@@H:18]2[OH:17])[CH2:28]1)[CH3:40]

Komponenten

5

Versuchsvorschrift

One equivalent of Jones Reagent is added to a solution of 3β-ethoxy-5-androstene-17β,19-diol 17-acetate in acetone at 10° C. After stirring for 30 minutes the acetone layer is poured onto cold water with vigorous stirring. The precipitate which forms is filtered, washed with water and dir dried. Crystallization of this precipitate from an ether-hexane mixture yields 3β-ethoxy-17β-hydroxy-5-androsten-19-one acetate.

Aufarbeitung

  1. filtrationThe precipitate which forms is filtered
  2. washwashed with water and dir
  3. customdried
  4. customCrystallization of this precipitate from an ether-hexane mixture

Quellen und Nachweise

ORD-Eintrag
ord-90c7acbf87e34c6dbf5dddf7d4f2e5ba
Quelldatensatz
uspto-grants-1979_02
Patentnummer
US04139617

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