Reacción #2146730

ord-a85275244d9546f49d326c5cdb4853d2

Ecuación de reacción

O=C1CCCCC1
cyclohexanone
Cl
HCl
[Li][C](C)(C)C
tert-butyllithium
CCCCC
pentane
CC(C)CI
isobutyl iodide
CC(C)CC1(O)CCCCC1
1-isobutylcyclohexanol

Disolventes

Condiciones de reacción

Temperatura
-70°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturawarmed to 10° C.
  2. 2
    Temperaturacooled to −70° C.
  3. 3
    workup.ADDITIONAt the end of the addition
  4. 4
    Otroto reach room temperature
  5. 5
    ExtracciónThe water phase was extracted with diethyl ether (300 ml)
  6. 6
    Lavadothe combined organic phases were washed with water (400 ml) and aqueous saturated NaCl solution (500 ml)
  7. 7
    Secadodried (50 g MgSO4)
  8. 8
    Otrothe solvent evaporated

Procedimiento

At −60° C., a solution of 1.7M tert-butyllithium in pentane (1000 ml, 1.7 mol, 2.1 eq.) in diethyl ether (800 ml) was treated dropwise within 1 h with isobutyl iodide (157 g, 0.81 mol, 1.0 eq.). The resulting solution was stirred at −70° C. for 45 min., warmed to 10° C., cooled to −70° C., and treated at this temperature within 4 h with cyclohexanone (100.7 ml, 0.971 mol, 1.2 eq.). At the end of the addition, the reaction mixture was allowed to reach room temperature before being poured into ice/H2O (500 ml) and acidified with concentrated HCl. The water phase was extracted with diethyl ether (300 ml) and the combined organic phases were washed with water (400 ml) and aqueous saturated NaCl solution (500 ml), dried (50 g MgSO4) and the solvent evaporated to give the crude 1-isobutylcyclohexanol (148 g).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08278230B2uspto-grants-2012_10