HCID 86733743, Verbindung → HCID 68128669, Verbindung
Reaktionsgleichung
[F:1][C@:2]12[C@@H:22]([OH:23])[CH2:21][C@@:20]3([CH3:24])[C@@H:12]([CH2:13][C@@H:14]([O:26][CH2:27][CH2:28][O:29]C4CCCCO4)[C@:15]3([OH:25])[C:16](=[O:19])[CH2:17][OH:18])[C@@H:11]1[CH2:10][CH2:9][C:8]1[C@:3]2([CH3:37])[CH2:4][CH2:5][C:6](=[O:36])[CH:7]=1>C(O)(=O)C.O>[F:1][C@:2]12[C@@H:22]([OH:23])[CH2:21][C@@:20]3([CH3:24])[C@@H:12]([CH2:13][C@@H:14]([O:26][CH2:27][CH2:28][OH:29])[C@:15]3([OH:25])[C:16](=[O:19])[CH2:17][OH:18])[C@@H:11]1[CH2:10][CH2:9][C:8]1[C@:3]2([CH3:37])[CH2:4][CH2:5][C:6](=[O:36])[CH:7]=1Komponenten
4
Edukt 1
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
A solution of 4.4 g of 9-fluoro-11β,17,21-trihydroxy-16α-[2-(tetrahydropyran-2-yloxy)ethoxy]pregn-4-ene-3,20-dione, 21-acetate in 60 ml each of acetic acid and water is stirred for 4 hours and the bulk of the solvent removed in vacuo. The residue is dissolved in chloroform and washed with 5% sodium bicarbonate solution. Drying and solvent removal gives an oil which crystallizes from acetone-hexane to give 2.4 g of 9-fluoro-11β,17,21-trihydroxy-16α-(2-hydroxyethoxy)pregn-4-ene-3,20-dione, 21-acetate, melting point 162°-165°C.
Aufarbeitung
- customthe bulk of the solvent removed in vacuo
- dissolutionThe residue is dissolved in chloroform
- washwashed with 5% sodium bicarbonate solution
- customDrying
- customsolvent removal
- customgives an oil which
- customcrystallizes from acetone-hexane
Quellen und Nachweise
- ORD-Eintrag
- ord-30f0f7478d204e149e03bf82f32cbdcc
- Quelldatensatz
- uspto-grants-1976_07
- Patentnummer
- US03971772
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