Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Phosphorus tribromide | HCID 24614 | — |
| Edukt | 1-Fluorenemethanol | HCID 52307 | — |
| Edukt | Fluorene-1-carboxylic acid | HCID 80468 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | (Bromo)(fluorenyl)methane | HCID 259258 | — |
Reaktionsschritte
Fluorene-1-carboxylic acid was purchased from Aldrich. It was reduced as described in J. Am. Chem. Soc. 1961, 83, 417 via the methyl ester to 1-hydroxymethylfluorene 1H NMR (CDCl3): δ 4.84 ppm (CH2), 3.89 ppm (CH2). 4.1 g (21 mmol) 1-hydroxymethylfluorene dissolved in 60 ml THF was slowly added to 2.54 g PBr3 in 10 ml THF at −5° C. The orange solution was stirred for 1.5 hrs at −5° C. then stirred for 16 hrs at room temperature. This was then poured into iced water, allowed to settle and 5.1 g of 1-bromomethylfluorene was isolated on a frit as an off-white powder. 1H NMR (CDCl3): δ 4.65 ppm (CH2), 3.97 ppm (CH2).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06369254B1 |
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| Quelldatensatz | uspto-grants-2002_04 |
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| ORD ID | ord-912acc061f8c4dde84f0f9a193a22e84 |
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| Quellennotiz | uspto-grants-2002_04 |
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