Reaktion #557865
ord-35c53c94a3d144fb8e07fab2a6f498c0
Reaktionsgleichung
Edukte
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1workup.STIRRINGthe resulting mixture was stirred at the same temperature for 30 minutes
- 2Einengenconcentrated under reduced pressure
- 3ExtraktionAfter extraction with ethyl acetate
- 4Waschenthe organic layer was washed with brine
- 5TrocknenThe organic layer was dried over anhydrous magnesium sulfate
- 6Filtrationfiltered
- 7Sonstigethe solvent in the filtrate was evaporated under reduced pressure
- 8SonstigeThe residue obtained
Vorschrift
1N sodium hydroxide solution (1.8 ml) was added to a methanol (10 ml) solution of the compound (1.00 g, 1.49 mmol) obtained in Step 1 of Example 108 and the resulting mixture was stirred at 70° C. for 5 hours. 65% Aqueous methanol (15 ml) solution of cerium (IV) diammonium nitrate (3.2 g, 5.96 mmol) was added dropwise to the reaction mixture under ice cooling and the resulting mixture was stirred at the same temperature for 30 minutes. Subsequently, the reaction mixture was rendered weakly acidic (pH 4 to 5) by addition of 1N sodium hydroxide solution and then concentrated under reduced pressure. After extraction with ethyl acetate, the organic layer was washed with brine. The organic layer was dried over anhydrous magnesium sulfate and filtered and then the solvent in the filtrate was evaporated under reduced pressure. The residue obtained was solidified by addition of diethyl ether to give 480 mg (65%) of the title compound as a solid.