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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1737147Generated: October 30, 2026

1-Methylcyclohexanecarboxylic acid → HCID 178421666, compound

https://huagongshe.com/reaction/1737147

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Methylcyclohexanecarboxylic acidHCID 70744—
ReactantAmmonium peroxysulphateHCID 9855511—
ReactantHCID 178516607HCID 178516607—
CatalystSilver NitrateHCID 24470—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventAcetonitrileHCID 6342—
ProductHCID 178421666HCID 17842166619.2%

Reaction Conditions

Temperature20 °C

Reaction Steps

To a stirred solution of 2-hydroxy-naphthalene-1,4-dione (1.00 g, 5.7 mmol), 1-methylcyclohexanecarboxylic acid (1.22 g, 8.6 mmol) and silver nitrate (600 mg) in a mixture of acetonitrile (20 ml) and water (20 ml) at 65° C. was slowly added a solution of ammonium peroxysulphate (1.96 g, 8.6 mmol) in water (10 ml) over a period of 15 minutes. The mixture was heated for a further hour before cooling to room temperature (about 20° C.) and diluting with diethyl ether (50 ml). The organic phase was separated and washed successively with water, dilute aqueous sodium hydrogen carbonate solution, water and saturated sodium chloride solution before drying over magnesium sulphate. Filtration and evaporation of the solvent under reduced pressure followed by silica gel column chromatography using 2:1 petrol:diethyl ether as eluant gave 2-hydroxy-3-(1-methyl-cyclohexyl)naphthalene-1,4-dione (296 mg) as a yellow crystalline compound, m.pt.: 79° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05962002
Source datasetuspto-grants-1999_10
ORD IDord-1d1f8cc128424d1786d6f53d18583f6c
Source noteuspto-grants-1999_10