HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Hydroxyacetophenone → 1-[3-(3-Phenylpropoxy)phenyl]ethan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Hydroxyacetophenone | HCID 8487 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (3-Bromopropyl)benzene | HCID 12503 | — |
| Catalyst | Sodium Iodide | HCID 5238 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-[3-(3-Phenylpropoxy)phenyl]ethan-1-one | HCID 21422440 | 94.4% |
Reaction Steps
3′-Hydroxyacetophenone (6.81 g, 50 mmol) and 1-bromo-3-phenyl propane (11.95 g, 60 mmol) were dissolved in dimethylformamide (70 ml). Then, potassium carbonate (15 g) and sodium iodide (0.5 g) were added thereto and the mixture was allowed to react for 7 hours at 80° C. Ethyl acetate (300 ml) and purified water (200 ml) were further added to the reaction mixture prior to stirring for 30 min. The organic layer extracted with ethyl acetate was dried over anhydrous magnesium sulfate, concentrated, and the resulting residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:5) to obtain the title compound (12.0 g, yield 94.2%) as a gel.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07741323B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-4521dbc84ec14ce1a4ca820a0481d911 |
| Source note | uspto-grants-2010_06 |