HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → 2,4-Dimethoxy-4b,5,6,8,8a-hexahydro-9(10H)-phenanthrone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Dimethyl Sulfate | HCID 6497 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,4-Dihydroxy-4b,6,7,8,8a,10-hexahydrophenanthren-9(5H)-one | HCID 20322774 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2,4-Dimethoxy-4b,5,6,8,8a-hexahydro-9(10H)-phenanthrone | HCID 5048382 | — |
Reaction Steps
To a flask equipped with a stirrer, dropping funnel, condenser, and gas inlet tube maintained under a nitrogen atmosphere, there is added 23.2 g (0.1 mole) of 2,4-dihydroxy-4b,5,6,7,8,8a,9,10-octahydro-9-oxo-phenanthrene, 20 g (0.15 mole) of dimethyl sulfate, 22 g (0.16 mole) of dry potassium carbonate and 500 ml of dry acetone, the resulting mixture is then refluxed with stirring overnight. The resulting suspension is cooled, 5 ml. of water is added and stirring is continued for an additional 5 minutes. The mixture is filtered, and the filtrate is concentrated to dryness. The resulting residue is recrystallized from acetone/methanol to give 2,4-dimethoxy-4b,5,6,7,8,8a,9,10-octahydro-9oxo-phenanthrene, m.p. 130°-131°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03976684 |
| Source dataset | uspto-grants-1976_08 |
| ORD ID | ord-acfff7ef65e4451da4c5b83bcd055721 |
| Source note | uspto-grants-1976_08 |