HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1030601Erstellt: 25. Oktober 2026
Water → 1,4-Dimethoxy-3-methylnaphthalene-2-carbaldehyde
https://huagongshe.com/reaction/1030601
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Water | HCID 962 | — |
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | 2-Bromo-1,4-dimethoxy-3-methylnaphthalene | HCID 292240 | — |
| Edukt | HCID 178418244 | HCID 178418244 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 1,4-Dimethoxy-3-methylnaphthalene-2-carbaldehyde | HCID 12847529 | 48,9% |
Reaktionsschritte
A solution cf 5.0 g (17.8 mmol) of 2-bromo-1,4-dimethoxy-3-methylnaphthalene in 30 ml of tetrahydrofuran was cooled to -78° C., to which 11.2 ml (17.9 mmol) of 1.6 M n-butyllithium hexane solution was added dropwise, and stirred at the same temperature for 10 minutes after completion of the addition. Then 1.3 g (17.8 mmol) of dimethylformamide was added dropwise to the reaction mixture, and stirred at room temperature for 1 hour after completion of the addition. Water was added to the reaction mixture, from which the product was extracted with ethyl acetate. The extract was washed with water, dried, and concentrated. The residue was purified with silica gel column chromatography (hexane-isopropyl ether (8:2)), and crystallized from hexane-isopropyl ether, to give 2.0 g (48.9%) of 2-formyl-1,4-dimethoxy-3-methylnaphthalene. m.p. 95°-96° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05106858 |
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| Quelldatensatz | uspto-grants-1992_04 |
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| ORD ID | ord-b7106b884e044ee5935831c20d61f62b |
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| Quellennotiz | uspto-grants-1992_04 |
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