Reaktion #1973903

Reaktionsgleichung

compound ( 23 )

8-[4-(4-butoxy-2,3-difluorophenyl)-cyclohexenyl]-1,4-dioxaspiro[4.5]decane

formic acid

water

→

4′-(4-butoxy-2,3-difluorophenyl)-bicyclohexyl-4-one

Ausbeute 98.5%

Lösungsmittel

toluene

toluene

Reaktionsbedingungen

Aufarbeitung

1. 1
   Temperaturthe mixture was heated
2. 2
   Temperaturto reflux for 2 hours
3. 3
   workup.ADDITIONmixed with it
4. 4
   Sonstigehad separated into two phases of organic and aqueous phases
5. 5
   Extraktionthe extraction into an organic phase
6. 6
   SonstigeThe resulting organic phase was separated
7. 7
   Waschenwashed successively with water
8. 8
   Trocknena saturated aqueous solution of sodium hydrogencarbonate and water, and then dried over anhydrous magnesium sulfate
9. 9
   workup.DISTILLATIONThen the solvent was distilled off under reduced pressure
10. 10
    Sonstigethe residue was purified by recrystallization from heptane solvent
11. 11
    Sonstigedried

Vorschrift

The compound (23) (7.7 g), formic acid (87%; 8.7 g) and toluene (100 ml) were mixed and the mixture was heated to reflux for 2 hours. After the reaction mixture had been cooled to 30° C., water (200 ml) and toluene (200 ml) were added to the mixture and mixed with it. The mixture was then allowed to stand until it had separated into two phases of organic and aqueous phases, and the extraction into an organic phase was carried out. The resulting organic phase was separated, and washed successively with water, a saturated aqueous solution of sodium hydrogencarbonate and water, and then dried over anhydrous magnesium sulfate. Then the solvent was distilled off under reduced pressure, and the residue was purified by recrystallization from heptane solvent and dried to give 4′-(4-butoxy-2,3-difluorophenyl)-bicyclohexyl-4-one (24) (6.8 g). The yield based on the compound (23) was 99.0%.

Quelle