Reacción #1746

Ecuación de reacción

methylene chloride

O-acetyl-4-phenylcyclohexanol

paraformaldehyde

Hydrogen chloride

→

trans-O-Acetyl-4-(4-chloromethylphenyl)-cyclohexanol

Disolventes

Condiciones de reacción

Tratamiento posterior

1. 1
   Otrorises to about 30° C.
2. 2
   Otroa substantially homogeneous solution is formed
3. 3
   Otroto react for 15 hours at ambient temperature
4. 4
   OtroThe organic phase is separated off
5. 5
   Extracciónthe aqueous phase is extracted with methylene chloride again
6. 6
   LavadoThey are washed until neutral,
7. 7
   Otrodried
8. 8
   Otroevaporated in vacuo
9. 9
   OtroThe yellow oil remaining is crystallised by trituration with diisopropylether
10. 10
    Otrothe solid product is recrystallised from diisopropylether
11. 11
    OtroWhite crystals are obtained

Procedimiento

A solution of 24.3 g (0.11 mol) of O-acetyl-4-phenylcyclohexanol in 1300 ml of methylene chloride is combined with 26.0 g (0.86 mol) of paraformaldehyde and 26.0 g (0.19 mol) of zinc chloride. Hydrogen chloride is introduced into this suspension, with stirring, for 2.5 hours, whilst the temperature rises to about 30° C. and a substantially homogeneous solution is formed. The mixture is then allowed to react for 15 hours at ambient temperature and the reaction mixture is then hydrolysed with stirring in about 1.5 litres of ice water. The organic phase is separated off, the aqueous phase is extracted with methylene chloride again and the two organic phases are combined. They are washed until neutral, dried and evaporated in vacuo. The yellow oil remaining is crystallised by trituration with diisopropylether and the solid product is recrystallised from diisopropylether. White crystals are obtained, melting point 87°-89° C.

Fuente