HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Tributylstannane → 1-(1-Benzofuran-3-yl)ethan-1-one
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Tributylstannane | HCID 5948 | — |
| Edukt | Azobisisobutyronitrile | HCID 6547 | — |
| Edukt | 1-(Benzofuran-3-yl)-2-bromoethanone | HCID 2776580 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 1-(1-Benzofuran-3-yl)ethan-1-one | HCID 11286612 | — |
Reaktionsschritte
A solution of 1-benzofuran-3-yl-2-bromo-ethanone (Intermediate I1) (commercially available from Maybridge) (2.1 g, 8.8 mmol) in toluene at reflux was treated with tributyltin hydride (2.9 mL, 10.6 mmol) and 2,2′-azobisisobutyronitrile (AIBN, catalyst) for 2 h. The mixture was cooled to rt and concentrated onto silica gel under reduced pressure. The product was eluted from a column of silica gel with 5% EtOAc: hexane to give 1-benzofuran-3-yl-ethanone (Intermediate I2) as an oil, 1.45 g (99%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07399868B2 |
| Quelldatensatz | uspto-grants-2008_07 |
| ORD ID | ord-c0c8f0438cd048dca0467085068bb4a6 |
| Quellennotiz | uspto-grants-2008_07 |