Reaktion #7952

Reaktionsgleichung

2-butyl-4-chloro-5-methoxy-2-(3-oxo-pentyl)-1-indanone

→

9a-butyl-8-chloro-7-methoxy-4-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-one

Ausbeute 60.6%

Lösungsmittel

EtOAc

acetic acid

HCl

Reaktionsbedingungen

Aufarbeitung

1. 1
   Waschenwashed with water (30 mL), 5% NaHCO3 (10 mL) and brine (5 mL)
2. 2
   Trocknendried over MgSO4
3. 3
   Filtrationfiltered
4. 4
   Sonstigeevaporated under vacuum to an oil (250 mg)
5. 5
   SonstigeThe crude product was purified by preparative layer chromatography on three 0.1×20×20 silica gel GF plates

Vorschrift

A solution of 2-butyl-4-chloro-5-methoxy-2-(3-oxo-pentyl)-1-indanone (250 mg, 0.74 mmol) in acetic acid (2 mL) was diluted with 6N aqueous HCl (2 mL). The resulting mixture was stirred and heated in an oil bath at 90° C. for 18 hours, then kept at room temperature for 2 days. The mixture was diluted with EtOAc (20 mL), washed with water (30 mL), 5% NaHCO3 (10 mL) and brine (5 mL), dried over MgSO4, filtered, and evaporated under vacuum to an oil (250 mg). The crude product was purified by preparative layer chromatography on three 0.1×20×20 silica gel GF plates, developing with 5% EtOAc in CH2Cl2, to afford 9a-butyl-8-chloro-7-methoxy-4-methyl-1,2,9,9a-tetrahydro-3H-fluoren-3-one (143 mg).

Quelle