Hydrochloric Acid → 68366-16-5

HRID 417792Notes

Reaction equation

HRID 417792 reaction equation
[C:1]([Li])([CH3:4])([CH3:3])[CH3:2].CCCCC.C(I)C(C)C.[C:16]1(=[O:22])[CH2:21][CH2:20][CH2:19][CH2:18][CH2:17]1.Cl>C(OCC)C>[CH2:2]([C:16]1([OH:22])[CH2:21][CH2:20][CH2:19][CH2:18][CH2:17]1)[CH:1]([CH3:4])[CH3:3]

Participants

7

Conditions

Temperature
-70 °C

Procedure

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).

Workup

  1. temperaturewarmed to 10° C.
  2. temperaturecooled to −70° C.
  3. additionAt the end of the addition
  4. customto reach room temperature
  5. extractionThe water phase was extracted with diethyl ether (300 ml)
  6. washthe combined organic phases were washed with water (400 ml) and aqueous saturated NaCl solution (500 ml)
  7. dry with materialdried (50 g MgSO4)
  8. customthe solvent evaporated

Sources & evidence

ORD record
ord-cc5bd6e57a2346749a19802f128c4c97
Source dataset
uspto-grants-2012_01
Patent number
US08093204B2

Reaction notes

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