HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Tributylstannane → 1-Fluoro-3-(4-chlorophenyl)-3-methyl-1-tributylstannyl-1-butene
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Tributylstannane | HCID 5948 | — |
| Edukt | Azobisisobutyronitrile | HCID 6547 | — |
| Edukt | 1-Fluoro-1-phenylsulfonyl-3-methyl-3-(4-chlorophenyl)-1-butene | HCID 53860513 | — |
| Lösungsmittel | Cyclohexane | HCID 8078 | — |
| Produkt | 1-Fluoro-3-(4-chlorophenyl)-3-methyl-1-tributylstannyl-1-butene | HCID 67632345 | — |
Reaktionsschritte
Under a nitrogen atmosphere, a stirring solution of 22.7 grams (0.067 mole) of 1-fluoro-1-phenylsulfonyl-3-methyl-3-(4-chlorophenyl)-1-butene, 42.0 grams (0.14 mole) of tributyltin hydride, and 0.5 gram (catalyst) of azobisisobutyronitrile in 700 mL of cyclohexane is heated at reflux for about three hours. After this time the reaction mixture is cooled to ambient temperature, and 125 mL of silica gel is added. The mixture is concentrated under reduced pressure, and the residue is subjected to column chromatography. The product-containing fractions are combined and concentrated under reduced pressure, yielding 1-fluoro-3-(4-chlorophenyl)-3-methyl-1-tributylstannyl-1-butene.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05622954 |
| Quelldatensatz | uspto-grants-1997_04 |
| ORD ID | ord-beee978054c2486f921e37cce4ee1d7b |
| Quellennotiz | uspto-grants-1997_04 |