Water → HCID 86736333, Verbindung
Reaktionsgleichung
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
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
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
- filtrationThe precipitate which forms is filtered
- washwashed with water and dir
- customdried
- 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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