HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 613866Erstellt: 26. Oktober 2026
Carbon tetrabromide → 3-(2,2-Dibromoethenyl)-2,5-dimethoxytetrahydrofuran
https://huagongshe.com/reaction/613866
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Carbon tetrabromide | HCID 11205 | — |
| Edukt | Triphenylphosphine | HCID 11776 | — |
| Edukt | Tetrahydro-2,5-dimethoxyfuran-3-carbaldehyde | HCID 567310 | — |
| Katalysator | Zinc | HCID 23994 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 3-(2,2-Dibromoethenyl)-2,5-dimethoxytetrahydrofuran | HCID 18380424 | 55,2% |
Reaktionsschritte
A mixture of Zn powder (1.65 g, 25.0 mmol), triphenylphosphine (6.54 g, 25.0 mmol), and CBr4 (8.30 g, 25.0 mmol) in dry CH2Cl2 (40 mL) was stirred at ambient temperature. After 24 hours, 2,5-dimethoxy-tetrahydrofuran-3-carboxaldehyde (2.00 g, 12.5 mmol) was added and an exothermic reaction ensued. After 30 minutes, pet ether (100 mL) was added and the resultant upper layer separated. The lower layer was twice diluted with CH2Cl2 (50 mL) and pet ether (50 mL), and the upper layer reserved. The combined upper layers were combined, passed through a pad of SiO2, and concentrated under reduced pressure at 30° C. or below to give 2.18 g (55%) of 3-(2,2-dibromoethenyl)-2,5-dimethoxytetrahydrofuran as a volatile colorless oil, which was a mixture of diastreomers by 1H NMR and used immediately without further purification.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06008243 |
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| Quelldatensatz | uspto-grants-1999_12 |
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| ORD ID | ord-70ff169213d541b0ba03153e63bc0a69 |
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| Quellennotiz | uspto-grants-1999_12 |
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