Reaktion #7937

Reaktionsgleichung

EtSH

AlCl3

HCl

NaHCO3

9a-butyl-7-methoxy-4-{4-[2-(1-piperidinyl)-ethoxy]phenyl}-1,2,9,9a-tetrahydro-3H-fluoren-3-one

→

9a-butyl-7-hydroxy-4-{4-[2-(1-piperidinyl)ethoxy]phenyl}-1,2,9,9a-tetrahydro-3H-fluoren-3-one

Lösungsmittel

EtOAc

water

tetrahydrofuran

CH2Cl2

Reaktionsbedingungen

Aufarbeitung

1. 1
   Sonstigecontained in an ice-cold flask
2. 2
   workup.WAITat room temperature for 35 minutes
3. 3
   TemperaturThe mixture was cooled in an ice bath
4. 4
   workup.STIRRINGstirred at 0° C. for 10 minutes
5. 5
   workup.STIRRINGstirred
6. 6
   SonstigeThe layers were separated
7. 7
   Extraktionthe aqueous portion extracted with EtOAc
8. 8
   WaschenThe combined organics were washed with brine
9. 9
   Trocknendried over MgSO4
10. 10
    Filtrationfiltered
11. 11
    Sonstigeevaporated under vacuum

Vorschrift

An ice-cold solution of 9a-butyl-7-methoxy-4-{4-[2-(1-piperidinyl)-ethoxy]phenyl}-1,2,9,9a-tetrahydro-3H-fluoren-3-one (85 mg, 96% weight pure, 0.172 mmol) in anhydrous CH2Cl2 (1.2 mL) was placed under a nitrogen atmosphere and treated with EtSH (0.055 mL, 0.743 mmol). The resulting solution was added by syringe to AlCl3 (115.2 mg, 0.864 mmol) contained in an ice-cold flask and kept under nitrogen. The resulting solution was stirred at 0° C. for 3 minutes, then at room temperature for 35 minutes. The mixture was cooled in an ice bath, treated with 0.5N HCl (1.6 mL) and tetrahydrofuran (1.0 mL), and stirred at 0° C. for 10 minutes. The resulting mixture was diluted with EtOAc (20 mL) and water (15 mL) and stirred while basifying with solid NaHCO3. The layers were separated and the aqueous portion extracted with EtOAc. The combined organics were washed with brine, dried over MgSO4, filtered, and evaporated under vacuum to afford 9a-butyl-7-hydroxy-4-{4-[2-(1-piperidinyl)ethoxy]phenyl}-1,2,9,9a-tetrahydro-3H-fluoren-3-one as a yellow semi-solid.

Quelle