Reacción #2126536

Ecuación de reacción

1-Ethoxy-2,3-difluoro-4-(trans-4-propylcyclohexyl)benzene

hydrobromic acid

acetic acid

Water

→

2,3-difluoro-4-(trans-4-propylcyclohexyl)phenol

Rendimiento 92.8%

Disolventes

toluene

Condiciones de reacción

Tratamiento posterior

1. 1
   Temperaturaunder reflux for 64 hours
2. 2
   Otroobtained
3. 3
   workup.ADDITIONmixed
4. 4
   Otrohad separated into an organic phase
5. 5
   OtroThe organic phase obtained
6. 6
   Lavadowashed with brine
7. 7
   Secadodried over anhydrous magnesium sulfate
8. 8
   workup.DISTILLATIONThe solvent was then distilled off under reduced pressure
9. 9
   Otrothe residue obtained
10. 10
    Otrowas purified by recrystallization from heptane
11. 11
    Otrodried

Procedimiento

1-Ethoxy-2,3-difluoro-4-(trans-4-propylcyclohexyl)benzene (5) (50.0 g), 48% hydrobromic acid (44.8 g), and glacial acetic acid (250 ml) were put in a reaction vessel, and stirred under reflux for 64 hours. After completion of the reaction had been confirmed by means of gas chromatographic analysis, the reaction mixture was cooled to 30° C. Water (500 ml) and toluene (500 ml) were added to the solution obtained, and mixed. Then, the mixture was allowed to stand until it had separated into an organic phase and an aqueous phase, and an extractive operation into an organic phase was carried out. The organic phase obtained was fractionated, washed with brine, and dried over anhydrous magnesium sulfate. The solvent was then distilled off under reduced pressure, and the residue obtained was purified by recrystallization from heptane and dried, giving 41.8 g of 2,3-difluoro-4-(trans-4-propylcyclohexyl)phenol (6). The yield based on the compound (5) was 92.9%.

Fuente