HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 433008Erstellt: 26. Oktober 2026
Allyl bromide → 1-Ferrocenyl-I-methyl-1,3-butadiene
https://huagongshe.com/reaction/433008
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Allyl bromide | HCID 7841 | — |
| Edukt | Hexane | HCID 8058 | — |
| Edukt | Magnesium | HCID 5462224 | — |
| Edukt | HCID 178466060 | HCID 178466060 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 1-Ferrocenyl-I-methyl-1,3-butadiene | HCID 131722479 | 91% |
Reaktionsschritte
72 mg (3.0 mmole) of magnesium metal was placed in a 50 ml round bottom flask. 228 mg (1.0 mmole) of ferrocenyl methyl ketone and 181.5 mg (1.5 mmole) of allyl bromide were dissolved in 15 ml of THF. The resulting mixture was poured into the round bottom flask containing the magnesium metal while stirring at room temperature for two hours. After two-hour stirring, the cover of the flask was opened, and the liquid portion of the reaction mixture was introduced into a silica gel column, which had been wetted with n-hexane. All the liquid migrated into the silica gel, and the column was placed still for 24 hours. Next, the column was eluated with n-hexane. After evaporating the solvent from the eluate collected from the elution, 230 mg (0.91 mmole) of a purified title product was obtained with a yield of 91%.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06664409B1 |
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| Quelldatensatz | uspto-grants-2003_12 |
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| ORD ID | ord-8fd3d17a05024ca185d17019e7633416 |
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| Quellennotiz | uspto-grants-2003_12 |
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