HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1180526Erstellt: 27. Oktober 2026
Dimethyl Sulfoxide → 2-Bromo-9,9-di-n-octylfluorene
https://huagongshe.com/reaction/1180526
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethyl Sulfoxide | HCID 679 | — |
| Edukt | 1-Bromooctane | HCID 8140 | — |
| Edukt | 2-Bromo-9H-fluorene | HCID 14336 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Katalysator | Benzyl triethylammonium chloride | HCID 66133 | — |
| Lösungsmittel | Hexane | HCID 8058 | — |
| Lösungsmittel | Diethylether water | HCID 21584184 | — |
| Produkt | 2-Bromo-9,9-di-n-octylfluorene | HCID 12964693 | 155,4% |
Reaktionsschritte
A 3L flask fitted with a mechanical stirrer was charged with 2-bromofluorene (45 g, 183.6 mmole) and 150 mL DMSO. Under a N2 atmosphere was added 80 mL of a 50% aqueous NaOH solution and 2.72 g of benzyl triethylammonium chloride (2.72 g, 11.98 mmole). This was stirred for 2 h at RT. With vigorous mechanical stirring, n-octylbromide (84.96 g, 440 mmole) was added via a dropping funnel (exotherm). Stirring was continued for 2 h. To the reaction mixture was added 500 mL of a 1:1 mixture of water/ether and the organic layer separated and washed successively with brine and then water. Drying over magnesium sulfate and evaporation of the solvent gave an oil. Purification by column chromatography (silica gel; hexane as the mobile phase) gave 67 g (78% yield) of 2-bromo-9,9-dioctylfluorene (9) as a pale oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07282275B2 |
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| Quelldatensatz | uspto-grants-2007_10 |
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| ORD ID | ord-f2a860accfa34c6bbea30a9467ba8c90 |
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| Quellennotiz | uspto-grants-2007_10 |
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