HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → 1-Fluoro-2-trifluoromethoxy-6-[(4-propylphenyl)ethynyl]naphthalene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 1-Ethynyl-4-propylbenzene | HCID 2775133 | — |
| Reactant | 2-Bromo-5-fluoro-6-trifluoromethoxynaphthalene | HCID 21870154 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-Fluoro-2-trifluoromethoxy-6-[(4-propylphenyl)ethynyl]naphthalene | HCID 21869758 | 36.6% |
Reaction Steps
10 g of 4-propyl-1-ethynylbenzene and 19.5 g of 2-bromo-5-fluoro-6-trifluoromethoxynaphthalene were dissolved in 50 ml of N,N-dimethylformamide (DMF). To the solution wore then added 50 mg of copper iodide (I) and 100 mg of tetrakis(triphenylphosphine)palladium (0). The reaction mixture was then stirred at room temperature for 5 hours. To the reaction solution was then added toluene. Insoluble matters were removed by filtration. The residue was then washed with water and saturated brine. The solvent was then distilled off. The residue was purified through silica gel column chromatography (hexane/ethyl acetate 9/1), and then recrystallized from ethanol to obtain 8.6 g of 1-fluoro-2-trifluoromethoxy-6-[(4-propylphenyl)ethynyl]naphthalene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06468607B1 |
| Source dataset | uspto-grants-2002_10 |
| ORD ID | ord-d1051ed337994ffba6ad130a04bb622a |
| Source note | uspto-grants-2002_10 |