HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Butyne → 2-But-1-ynyl-4-fluorophenylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Butyne | HCID 7846 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 4-Fluoro-2-iodoaniline | HCID 2778283 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 2-But-1-ynyl-4-fluorophenylamine | HCID 58080372 | — |
Reaction Steps
80 ml of tetrahydrofuran is placed under argon. 5 g 4-fluoro-2-iodophenylamine, 0.74 g dichlorobis(triphenylphosphine) palladium(II), 0.2 g copper iodide and 8.8 ml triethylamine are added. 4 g gaseous 1-butyne are passed through the suspension. The reaction mixture is stirred under argon for 15 hours at ambient temperature, then filtered through Celite and evaporated to dryness. 3.4 g product are obtained in the form of a solid. 1H NMR (400 MHz, DMSO): 2.45 (2H, q); 1.18 (3H, t).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09161927B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-72be47ac980441c8a82a26bc0fd26d7d |
| Source note | uspto-grants-2015_10 |