HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Allyl bromide → 1,3-Butadienylferrocene
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Allyl bromide | HCID 7841 | — |
| Edukt | Ferrocenecarboxyaldehyde | HCID 15184314 | — |
| Edukt | HCID 178450094 | HCID 178450094 | — |
| Edukt | HCID 178466060 | HCID 178466060 | — |
| Katalysator | Magnesium | HCID 5462224 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | 1,3-Butadienylferrocene | HCID 129665232 | — |
Reaktionsschritte
Ferrocenaldehyde or ferrocenyl methyl ketone and allyl bromide are reacted in an ether solvent and in the presence of magnesium metal as a catalyst. The liquid portion of the reaction mixture is introduced into a silica gel column, wherein the weak acidity of the silica gel is able to dehydrate the reaction intermediate 1-ferrocenyl-3-buten-1-ol product. The column is eluted with n-hexane, and after evaporating the solvent from the eluate collected, a purified ferrocenyl-1,3-butadiene product is obtained.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06664409B1 |
| Quelldatensatz | uspto-grants-2003_12 |
| ORD ID | ord-1873e47b27344b03a5faf5cb04c75af6 |
| Quellennotiz | uspto-grants-2003_12 |