Ethanol → Methyl 4-hydroxy-1-methylcyclohexane-1-carboxylate

HRID 1788377Notes

Reaction equation

HRID 1788377 reaction equation
[CH3:1][O:2][C:3]([C:5]1([CH3:12])[CH2:10][CH2:9][C:8](=[O:11])[CH2:7][CH2:6]1)=[O:4].CO.C(O)C.[BH4-].[Na+]>O>[CH3:1][O:2][C:3]([C:5]1([CH3:12])[CH2:10][CH2:9][CH:8]([OH:11])[CH2:7][CH2:6]1)=[O:4]

Participants

6

Conditions

Temperature
0 °C

Procedure

To a solution of 3.7 g (20.1 mmol) of 1-methyl-4-oxocyclohexanecarboxylic acid methyl ester in mixture of methanol and ethanol (6 mL+15 mL) was added 200 mg (5.29 mmol) of sodium borohydride at 0° C., and stirred for 1 hour at 0° C. After addition of water thereto, the reaction mixture was concentrated under a reduced pressure and the residue was extracted with ethyl acetate. The organic layer was washed with water and saturated brine successively and dried over anhydrous magnesium sulfate. Upon removal of the solvent by evaporation, 3.8 g (yield 100%) of 4-hydroxy-1-methylcyclohexanecarboxylic acid methyl ester was obtained as colorless liquid. Its physical property is shown below.

Workup

  1. concentrationthe reaction mixture was concentrated under a reduced pressure
  2. extractionthe residue was extracted with ethyl acetate
  3. washThe organic layer was washed with water and saturated brine successively
  4. dry with materialdried over anhydrous magnesium sulfate
  5. customUpon removal of the solvent
  6. customby evaporation

Sources & evidence

ORD record
ord-74feaf0457f54e15a04898127b057169
Source dataset
uspto-grants-2009_03
Patent number
US07511144B2

Reaction notes

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