HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylamine → 2-Amino-4-phenylethynyl-thiophene-3-carboxylic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | Iodobenzene | HCID 11575 | — |
| Reactant | 2-Amino-4-ethynyl-thiophene-3-carboxylic acid ethyl ester | HCID 86030821 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-Amino-4-phenylethynyl-thiophene-3-carboxylic acid ethyl ester | HCID 69607374 | 78% |
Reaction Steps
2-Amino-4-ethynyl-thiophene-3-carboxylic acid ethyl ester (0.075 g, 0.385 mmol) was dissolved in anhydrous CH3CN (2.0 mL). This was treated with iodobenzene (0.129 mL, 1.15 mmol) followed by diisopropylamine (0.272 mL, 1.92 mmol). The solution was then degassed and treated with copper iodide (0.0018 g, 0.010 mmol) and dichlorobis(triphenylphosphine)palladium(II) (0.014 g, 0.019 mmol). The reaction was then stirred at room temperature for 30 min. The reaction was concentrated in vacuo. The crude product was purified by flash chromatography (SiO2, 15 EtOAc/85 hexanes) to afford the title compound (0.081 g, 78%). MS m/e (CI) 272.0 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07119205B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-1353930791ae4fc8af2e7ac1132d4775 |
| Source note | uspto-grants-2006_10 |