HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1737147Generated: October 30, 2026
1-Methylcyclohexanecarboxylic acid → HCID 178421666, compound
https://huagongshe.com/reaction/1737147
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Methylcyclohexanecarboxylic acid | HCID 70744 | — |
| Reactant | Ammonium peroxysulphate | HCID 9855511 | — |
| Reactant | HCID 178516607 | HCID 178516607 | — |
| Catalyst | Silver Nitrate | HCID 24470 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178421666 | HCID 178421666 | 19.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05962002 |
|---|
| Source dataset | uspto-grants-1999_10 |
|---|
| ORD ID | ord-1d1f8cc128424d1786d6f53d18583f6c |
|---|
| Source note | uspto-grants-1999_10 |
|---|