HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 33416Erstellt: 25. Oktober 2026
Ethanol → Methyl 9-methylfluorene-9-carboxylate
https://huagongshe.com/reaction/33416
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethanol | HCID 702 | — |
| Edukt | Diethyl Ether | HCID 3283 | — |
| Edukt | Methyl iodide | HCID 6328 | — |
| Edukt | 9-Carboxyfluorene | HCID 74809 | — |
| Edukt | Sodium | HCID 5360545 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | Methyl 9-methylfluorene-9-carboxylate | HCID 14934655 | — |
Reaktionsschritte
From 7.6 g (0.33 mol) of sodium and 300 mL of ethanol, a sodium ethoxide solution is prepared, to which 69.6 g (0.33 mol) of 9-fluorenecarboxylic acid are added batchwise. After the addition has ended, the mixture is stirred for 2.5 hours at ambient temperature. Then it is evaporated to dryness, the residue is suspended in 600 mL of dimethylformamide, and 93.96 g (0.662 mol) of methyl iodide are added dropwise. The mixture is stirred for 3 hours at constant temperature. The cloudy solution is stirred into 500 mL of water and 300 mL of diethyl ether with cooling and extracted, the organic phase is washed with water and 10% sodium carbonate solution, dried, and evaporated to dryness. The residue is purified by column chromatography, eluent: cyclohexane-ethyl acetate (96:4). Yield: 12.61 g of white crystals (16% of theoretical yield); melting point: 108° C.-109° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07429600B2 |
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| Quelldatensatz | uspto-grants-2008_09 |
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| ORD ID | ord-8d3d2567e946411abba258d8b76140a6 |
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| Quellennotiz | uspto-grants-2008_09 |
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