HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 6-(12-Acetoxydodecyl)-2,3-dimethoxy-5-methyl-1,4-benzoquinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Monobasic potassium phosphate | HCID 516951 | — |
| Reactant | Potassium nitrosodisulfonate | HCID 3032624 | — |
| Reactant | 6-(12-Acetoxydodecyl)-2,3-dimethoxy-5-methylphenol | HCID 13065236 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-(12-Acetoxydodecyl)-2,3-dimethoxy-5-methyl-1,4-benzoquinone | HCID 12881465 | 76% |
Reaction Steps
To a solution (300 ml) of 6-(12-acetoxydodecyl)-2,3-dimethoxy-5-methylphenol (6.1 g) in dimethylformamide are added potassium nitrosodisulfonate (18 g), water (300 ml), methanol (50 ml) and potassium dihydrogen phosphate (0.5 g), and the mixture is stirred at room temperature for 30 days. The product is extracted with dichloromethane, and the organic layer is washed with water and dried over anhydrous magnesium sulfate. The solvent is distilled off to give crude crystals. This product is recrystallized from hexane to give orange-yellow needles of 6-(12-acetoxydodecyl)-2,3-dimethoxy-5-methyl-1,4-benzoquinone (4.8 g). m.p. 47° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04436753 |
| Source dataset | uspto-grants-1984_03 |
| ORD ID | ord-a5569572ad524e3e943bfd9d4830af3e |
| Source note | uspto-grants-1984_03 |