Reacción #833548

ord-aaf271fcf2e345e0aff63f8e9b08bf0c

Ecuación de reacción

[Al+3].[H-].[H-].[H-].[H-].[Li+]
LAH
CC(=O)C1=CCCC(C)(C)C1
1-(5′,5′-dimethylcyclohex-1′-enyl)ethanone
CC(O)C1=CCCC(C)(C)C1
1-(5′,5′-dimethylcyclohex-1′-enyl)ethanol
Rendimiento 85.0%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaThe reaction mixture was refluxed for 1 h
  2. 2
    Otroto quenching at 0° C. by careful addition of water (50 ml)
  3. 3
    OtroThe organic layer was separated
  4. 4
    Extracciónthe aqueous one extracted with Et2O
  5. 5
    LavadoThe combined ethereal solutions were washed with water and brine
  6. 6
    Secadodried (Na2SO4)
  7. 7
    Concentraciónconcentrated in a rotary evaporator

Procedimiento

A solution of 1-(5′,5′-dimethylcyclohex-1′-enyl)ethanone (13.1 g, 85.8 mmol) in Et2O (50 ml) was added dropwise with stirring within 50 min. to a suspension of LAH (895 mg, 23.6 mmol) in Et2O (150 ml). The reaction mixture was refluxed for 1 h prior to quenching at 0° C. by careful addition of water (50 ml) followed by 5 N aq. HCl (50 ml). The organic layer was separated and the aqueous one extracted with Et2O. The combined ethereal solutions were washed with water and brine, dried (Na2SO4), and concentrated in a rotary evaporator. Silica-gel FC (pentane/Et2O, 9:1, Rf=0.14) of the resulting residue (14.7 g) gave 11.2 g (85%) of 1-(5′,5′-dimethylcyclohex-1′-enyl)ethanol.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07393822B2uspto-grants-2008_07