HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1528034Erstellt: 24. Oktober 2026
4-Bromo-2-methylbut-1-ene → 2-Methoxy-1-[2,4,6-trihydroxy-3,5-di(3-methyl-2-buten-1-yl)phenyl]ethanone
https://huagongshe.com/de/reaction/1528034
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 4-Bromo-2-methylbut-1-ene | HCID 549585 | — |
| Edukt | 2-Methoxy-1-(2,4,6-trihydroxyphenyl)ethanone | HCID 643400 | — |
| Lösungsmittel | Potassium Hydroxide | HCID 14797 | — |
| Produkt | 2-Methoxy-1-[2,4,6-trihydroxy-3,5-di(3-methyl-2-buten-1-yl)phenyl]ethanone | HCID 86702215 | 41% |
Reaktionsschritte
2-methoxy-1-(2,4,6-trihydroxyphenyl)ethanone (8.3 g, 42 mmol) was dissolved in a 5% potassium hydroxide aqueous solution (84 ml). After the reaction mixture was cooled below 0° C., Isopentenyl bromide (12.48 g, 84 mmol) was slowly added dropwise to within 30 minutes. The reaction mixture was stirred at room temperature (RT) for 2 hours, then poured into an ice water and acidified to pH 2. The reaction mixture was extracted with ethyl acetate. The extract was collected and dried over anhydrous sodium sulfate, followed by removing solvent. The desired compound was obtained by purifying the residue by silica gel column chromatography (dichloromethane as eluent) (5.7 g, yield 41%). 1H NMR (400 MHz, DMSO-d6): δ=11.44 (s, 2H), 9.24 (s, 1H), 5.00 (t, 2H, J=6.8 Hz), 4.63 (s, 2H,), 3.31 (s, 3H), 3.22 (d, 4H, J=6.8 Hz), 1.67 (s, 6H), 1.58 (s, 6H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09090583B2 |
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| Quelldatensatz | uspto-grants-2015_07 |
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| ORD ID | ord-53f269416ed1433b81d3fd78cfd8b932 |
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| Quellennotiz | uspto-grants-2015_07 |
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