HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-(5-(3-Bromophenyl)pent-4-ynyl)isoindoline-1,3-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Bromo-3-fluorobenzene | HCID 14082 | — |
| Reactant | N-(4-Pentynyl)phthalimide | HCID 11769822 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(5-(3-Bromophenyl)pent-4-ynyl)isoindoline-1,3-dione | HCID 67203127 | — |
Reaction Steps
1-Bromo-3-fluoro-benzene (1.0 mL, 7.8 mmol), 2-pent-4-ynyl-isoindole-1,3-dione (1.8 g, 8.6 mmol), Pd(PPh3)2Cl2 (191 mg, 0.27 mmol), CuI (118 mg, 0.62 mmol), and triethylamine (4.4 mL, 31.3 mmol) were taken up into DMF (10 mL) and stirred at room temperature for four hours. The reaction was then quenched with saturated NaHCO3 and the resulting mixture extracted with EtOAc and washed with brine, then dried over sodium sulfate and the solvent removed in vacuo. The resulting residue was purified on normal phase chromatography (Heptane/EtOAc) to yield 2-(5-(3-bromophenyl)pent-4-ynyl)isoindoline-1,3-dione. MH+ 368, 370
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08633322B2 |
| Source dataset | uspto-grants-2014_01 |
| ORD ID | ord-e7447d44287547cbbed70defc7eb2690 |
| Source note | uspto-grants-2014_01 |