Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015657Generated: October 30, 2026

Sodium Hydroxide → (1r,2s,4r)-2-Hydroxy-4-methylcyclohexanecarboxylic acid

https://huagongshe.com/reaction/1015657

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantHCID 67299189HCID 67299189—
SolventMethanolHCID 887—
Product(1r,2s,4r)-2-Hydroxy-4-methylcyclohexanecarboxylic acidHCID 4508490782%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of (1R,2S,4R)-2-Hydroxy-4-methyl-cyclohexanecarboxylic acid methyl ester (450 mg, 2.42 mmol) in methanol (12 ml) was added a 2.5 M solution of sodium hydroxide (9.7 ml, 24.2 mmol). The reaction mixture was stirred for 4 h at 50° C. Then, the solvents were removed and the residue was partitioned between 20 ml of H2O acidified to pH 4 and 20 ml of EtOAc. The organic layer was separated and the aqueous phase was washed with ethyl acetate (2×20 ml). The combined ethyl acetate layers were dried (Na2SO4) and concentrated to obtain 313 mg (82%) of (1R,2S,4R)-2-Hydroxy-4-methyl-cyclohexanecarboxylic acid. NMR 1H (CDCl3, 400 MHz) 4.34 ppm (s, 1H); 2.43-2.39 ppm (m, 1H); 1.96-1.76 ppm (m, 5H); 1.14-1.08 ppm (m, 1H); 1.02-0.93 ppm (m, 1H); 0.90 ppm (d, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07985769B2
Source datasetuspto-grants-2011_07
ORD IDord-1396eca061054da4b3292c7544d540a9
Source noteuspto-grants-2011_07