Reaktion #1973905

Reaktionsgleichung

toluene

compound ( 16 )

trans-4-(4-Ethoxy-2,3-difluorophenyl)-cyclohexanecarboaldehyde

acetone

Jones reagent

→

4-ethoxy-2,3-difluoro-(trans-4-cyclohexyl)-carboxylic acid

Lösungsmittel

water

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.STIRRINGthe mixture was stirred at 35° C. for 2 hours
2. 2
   TemperaturAfter the reaction mixture had been cooled to 30° C.
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
   Trocknenan aqueous solution of sodium thiosulfate and water, and then dried over anhydrous magnesium sulfate

Vorschrift

The compound (16) (10.0 g) and acetone (50 ml) were mixed and the mixture was stirred at 35° C. for 30 minutes. Jones reagent (8N) (4.7 ml) was added to the mixture in the temperature range of 30 to 40° C. and the mixture was stirred at 35° C. for 2 hours. After the reaction mixture had been cooled to 30° C., toluene (200 ml) and water (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, an aqueous solution of sodium thiosulfate and water, and then dried over anhydrous magnesium sulfate, giving 4-ethoxy-2,3-difluoro-(trans-4-cyclohexyl)-carboxylic acid (31) (8.8 g). The yield based on the compound (16) was 83.1%.

Quelle