Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Fluorene-2-carboxaldehyde | HCID 34804 | — |
| Edukt | Triphenylmethyl phosphonium bromide | HCID 21951224 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Hexane | HCID 8058 | — |
| Produkt | 2-ethenyl-9H-fluorene | HCID 11041607 | — |
Reaktionsschritte
Triphenylmethyl phosphonium bromide (36 gms/0.1 mole) in 500 milliliters of dry THF is treated under nitrogen with 90 milliliters of a 1.1 molar solution of n-butyl lithium in hexane and stirred for 2 hours. A solution of 19.4 gms. (0.1 mole) of fluorene-2-carboxaldehyde in 100 milliliters of THF is added dropwise and the final mixture refluxed for 11/2 hours. One liter of hexane is added to the cold solution and the precipitate filtered off. The filtrate is evaporated and the residue chromatographed on alumina (Woehlm neutral) using hexane to give 15 gms. (75% theory) of product. Recrystallization from hexane yields 2-vinylfluorene as colorless plates. The structure of the product is confirmed by nuclear magnetic resonance and elemental analysis.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04011266 |
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| Quelldatensatz | uspto-grants-1977_03 |
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| ORD ID | ord-0da5f13a5e9a40c78ab8d905c83a7eb5 |
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| Quellennotiz | uspto-grants-1977_03 |
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