HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Phenylacetophenone → Benzofurans
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Phenylacetophenone | HCID 9948 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 1,2-Dibromobenzene | HCID 11414 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | Benzofurans | HCID 253613 | 80.7% |
Reaction Steps
39.2 g of benzyl phenyl ketone, 46.7 g of 1,2-dibromobenzene, g of palladium acetate, 10.5 g of triphenylphosphine, 77.2 g of cesium carbonate, and 400 mL of o-xylene were loaded into a flask, and the mixture was refluxed and stirred under heat under an argon atmosphere for 8 hours. After the completion of the reaction, the reaction solution was filtrated while being extracted with ether. The filtrate was dried with magnesium sulfate, and was then concentrated. The residue was purified by silica gel column chromatography, whereby 43.2 g of a white crystal were obtained (80% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08512875B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-0b22d1ef6f82485cb7e16e9087c5a57c |
| Source note | uspto-grants-2013_08 |