Reacción #1392

ord-822a168440d44234b23b8b29fa23f00d

Ecuación de reacción

COc1cccc(C2(O)CCCCC2CN(C)C)c1.Cl
(1RS,2RS)-2-dimethylaminomethyl-1-(3-methoxy-phenyl)-cyclohexanol hydrochloride
[Na+].[OH-]
caustic soda
COc1cccc(C2(O)CCCCC2CN(C)C)c1
(1RS,2RS)-2-dimethylaminomethyl-1-(3-methoxy-phenyl)-cyclohexanol
Rendimiento 99.9%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONtreated with 1.6 kg
  2. 2
    Otrocrushed ice
  3. 3
    ExtracciónThe mixture was subsequently extracted with 7000 ml dichloromethane
  4. 4
    Extracciónwas extracted with a further 2000 ml dichloromethane
  5. 5
    Otroafter phase separation
  6. 6
    SecadoThe combined organic phases were dried over sodium sulphate
  7. 7
    OtroAfter removing the solvent
  8. 8
    workup.DISTILLATIONby distillation

Procedimiento

3 kg (10 mole) (1RS,2RS)-2-dimethylaminomethyl-1-(3-methoxy-phenyl)-cyclohexanol hydrochloride (1) were suspended in 4800 ml water and treated with 1.6 kg crushed ice. 1300 ml of 36-38% (technical) caustic soda solution were added drop-wise with stirring. The mixture was subsequently extracted with 7000 ml dichloromethane, and was extracted with a further 2000 ml dichloromethane after phase separation. The combined organic phases were dried over sodium sulphate. After removing the solvent by distillation, 2630 g (99% theoretical) of (1RS,2RS)-2-dimethylaminomethyl-1-(3-methoxy-phenyl)-cyclohexanol were obtained as a syrup.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US05723668uspto-grants-1998_03