Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Butyn-1-OL | HCID 13566 | — |
| Reactant | Aluminum | HCID 5359268 | — |
| Reactant | HCID 59790308 | HCID 59790308 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 59305318 | HCID 59305318 | 82.4% |
Reaction Steps
In a 0.5-2 ml Biotage conical microwave vial equipped with magnetic spin vane was dissolved 1-(3-Bromo-4-fluoro-phenyl)-2-(4-difluoromethoxy-phenyl)-ethane-1,2-dione (100 mg, 0.268 mmol) in triethylamine (1.25 mL). Copper iodide (10 mg, 0.052 mmol) and Tetrakis(triphenylphosphine) palladium (20 mg, 0.017 mmol) were added. Lastly But-3-yn-1-ol (100 mg, 1.04 mmol) was added, the vial was covered with a teflon septa, an aluminum cap was crimped in place, and the assembly was set on a Biotage Emrys microwave instrument to irradiate at 80° C. for one hour. The crude reaction was diluted with diethylether (60 mL), washed with saturated ammonium chloride (2×30 mL) and purified via column chromatography on a Yamazen W-Prep 2XY using a two-step automatic gradient elution: 100% hexanes (4 min) to 18% EtOAc (12 min), hold 4 min then to 80% EtOAc (16 min) hold 15 minutes. The resultant oil was placed under high vacuum overnight to afford 80 mgs of beige solid (82%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07723368B2 |
|---|
| Source dataset | uspto-grants-2010_05 |
|---|
| ORD ID | ord-1ff5055e7ddc41cdbf72cb3e94923974 |
|---|
| Source note | uspto-grants-2010_05 |
|---|