HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 720018Erstellt: 26. Oktober 2026
Dimethylformamide → 2-Bromo-9,9-dimethoxyethylfluorene
https://huagongshe.com/reaction/720018
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | 2-Bromo-9H-fluorene | HCID 14336 | — |
| Edukt | 2-Bromoethyl methyl ether | HCID 80972 | — |
| Edukt | Potassium tert-butoxide | HCID 23665647 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 2-Bromo-9,9-dimethoxyethylfluorene | HCID 69587088 | — |
Reaktionsschritte
To a solution of 2-bromofluorene (2.0 g, 8.2 mmol) in dimethylformamide (dry, 30 ml) was added potassium t-butoxide (2.74 g, 24.4 mmol), giving a deep orange in color. The mixture was stirred at 45° C. for 20 min and added 2-bromoethylmethyl ether (3.5 g, 2.5 mmol) dropwise. Stirring was continued at the same temperature for overnight to give an orange solution. Another portion of 2-bromoethylmethyl ether (1.4 g, 1.0 mmol) was added and the mixture stirred at 80° C. for 4 h. It was diluted with water (100 ml). The products extracted with ethylacetate (20 ml) and washed with water. Organic layer was dried over magnesium sulfate and concentrated in vacuuo to afford the crude product. It was purified by preparative thin layer chromatography (silica gel, Rf=0.3 using hexane-EtOAc/3:2 as eluent) to give 2-bromo-9,9-dimethoxyethylfluorene (1.5 g).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07132572B2 |
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| Quelldatensatz | uspto-grants-2006_11 |
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| ORD ID | ord-dc989689314d4eefbdcd9bd4ab551516 |
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| Quellennotiz | uspto-grants-2006_11 |
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