HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 69670919, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Phenylacetylene | HCID 10821 | — |
| Reactant | Iodide Ion | HCID 30165 | — |
| Reactant | 2-Bromo-4-(trifluoromethoxy)aniline | HCID 688296 | — |
| Catalyst | HCID 178419050 | HCID 178419050 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 69670919 | HCID 69670919 | — |
Reaction Steps
To a mixture of 2-bromo-4-trifluoromethoxyaniline (0.500 g), cupper iodide (I) (18.6 mg), bis(triphenylphosphine)palladium (II) dichloride (68.5 mg), triethylamine (0.817 mL) and tetrahydrofuran (7.8 mL) was added phenylacetylene (0.279 mL) at room temperature under stirring, and the mixture was stirred at 80° C. for 16 hours. The reaction mixture was cooled to room temperature, diluted with diethyl ether (30 mL) and then filtered through celite (registered trademark). The filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluting solvent: ethyl acetate-hexane) to obtain the title compound (206 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08680120B2 |
| Source dataset | uspto-grants-2014_03 |
| ORD ID | ord-d9926286bda947c58406469e41ab52f6 |
| Source note | uspto-grants-2014_03 |