HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1193025Erstellt: 26. Oktober 2026
Furfural → ([4-Bromo-2,6-dimethylphenyl]furan-2-yl)methanol
https://huagongshe.com/reaction/1193025
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Furfural | HCID 7362 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | 5-Bromo-2-iodo-1,3-dimethylbenzene | HCID 2735573 | — |
| Edukt | HCID 178418918 | HCID 178418918 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | ([4-Bromo-2,6-dimethylphenyl]furan-2-yl)methanol | HCID 66709611 | 82,5% |
Reaktionsschritte
4-Bromo-2,6-dimethyl-1-iodobenzene (5 g, 16 mmol) is dissolved in dry tetrahydrofuran (20 ml) and cooled to −78° C. under an atmosphere of dry nitrogen. Isopropylmagnesium chloride (2M solution in tetrahydrofuran, 10 ml, 20 mmol) is added dropwise with vigorous stirring over 30 minutes. When the addition is complete, the reaction is allowed to warm to room temperature and is stirred for 30 minutes at room temperature. The reaction mixture is cooled to −78° C. and a solution of 2-furaldehyde (2.4 g, 25 mmol) in dry tetrahydrofuran (10 ml) is added dropwise over 30 minutes. Once the addition is complete, the mixture is allowed to warm to room temperature and stirring continued for 2 hours. A solution of saturated aqueous ammonium chloride (30 ml). is added, and the mixture is extracted with dichloromethane (3×25 ml). The organic extracts are combined, washed with brine, dried over anhydrous magnesium sulfate, filtered and the filtrate is evaporated under reduced pressure. The residue is purified by column chromatography on silica gel to give ([4-bromo-2,6-dimethylphenyl]furan-2-yl)methanol (3.71 g).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08680339B2 |
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| Quelldatensatz | uspto-grants-2014_03 |
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| ORD ID | ord-0be7fb479df94a41b7e743df13130fc0 |
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| Quellennotiz | uspto-grants-2014_03 |
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