HuagongsheHuagongshe Chemistry Print Report · For research reference only
Anthrone → Ethanol, 2-(9-anthracenyloxy)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Anthrone | HCID 7018 | — |
| Reactant | 2-Bromoethanol | HCID 10898 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethanol, 2-(9-anthracenyloxy)- | HCID 11265428 | — |
Reaction Steps
To a solution of anthrone (5.0 g, 25.7 mmole) in 34 mL anhydrous DMF under an inert atmosphere was added potassium carbonate (7.47 g, 54.1 mmole). To the resulting reaction mixture was added 2-bromoethanol (2.0 mL, 28.3 mmole). The resulting reaction mixture was stirred for 1 hr at room temperature, then 3 hrs at 80° C. The reaction was then cooled to room temperature and quenched with saturated NaHCO3. Ethyl acetate was added and the organic layer was collected and dried over magnesium sulfate. The solvent was concentrated under reduced pressure and the residue was purified via flash chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09234153B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-5d7b9a263d86414abb91f2db5d548325 |
| Source note | uspto-grants-2016_01 |