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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1788377Generated: November 3, 2026

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

https://huagongshe.com/reaction/1788377

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantMethanolHCID 887—
ReactantSodium borohydrideHCID 4311764—
ReactantMethyl 1-methyl-4-oxocyclohexane-1-carboxylateHCID 12568255—
SolventWaterHCID 962—
ProductMethyl 4-hydroxy-1-methylcyclohexane-1-carboxylateHCID 13236236109.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07511144B2
Source datasetuspto-grants-2009_03
ORD IDord-74feaf0457f54e15a04898127b057169
Source noteuspto-grants-2009_03