HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → 2,6-dimethoxyanthraquinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | 2,6-Dihydroxyanthraquinone | HCID 6776 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Product | 2,6-dimethoxyanthraquinone | HCID 4589998 | — |
Reaction Steps
To a suspension of 2,6-dihydroxyanthraquinone (3 g, 12.5 mmole) and anhydrous potassium carbonate (23 g) in acetone (400 ml), dimethyl sulfate (20 g, 158 mmole) was added at room temperature. The resulting mixture was reacted with stirring for 6 hours under reflux. After standing at room temperature overnight, the reaction mixture was poured into cold H2O (580 ml). The precipitate was filtered and dried. The resultant crude dark brown solid (3.1 g) was recrystallized from benzene to give 2.7 g of 2,6-dimethoxyanthraquinone as yellow-brown crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05498748 |
| Source dataset | uspto-grants-1996_03 |
| ORD ID | ord-ce2fc24b4bbc476e947e03133d9e7394 |
| Source note | uspto-grants-1996_03 |