HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,10-Phenanthroline → HCID 22137973, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,10-Phenanthroline | HCID 1318 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 4-Fluorobenzylic alcohol | HCID 68022 | — |
| Reactant | 1-(2-Fluoro-4-iodophenyl)-2,5-dimethyl-1H-pyrrole | HCID 15354630 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 22137973 | HCID 22137973 | 75.1% |
Reaction Steps
A solution of 1-(2-fluoro-4-iodo-phenyl)-2,5-dimethyl-1H-pyrrole (33.18 g, 105 mmol), 4-fluorobenzylalcohol (26.6 g, 211 mmol), cesium carbonate (68.6 g, 211 mmol), cuprous iodide (2.0 g, 11 mmol) and 1,10-phenanthroline (3.8 g, 21 mmol) in toluene (52 mL) was heated at 100° C. in an autoclave for 48 h. After cooling to room temperature, the mixture was filtered and poured into sodium hydroxide (1N). The resulting mixture was extracted with toluene and the organic extracts washed with brine, dried and evaporated. The residue was triturated with boiling hexane to leave the title compound (24.7 g, 75%) as a light brown solid. MS: m/e=314.1 (M++H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07053245B2 |
| Source dataset | uspto-grants-2006_05 |
| ORD ID | ord-ef906712429d47229a39ee28fda5f928 |
| Source note | uspto-grants-2006_05 |