HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 550239Erstellt: 24. Oktober 2026
Dimethylformamide → 4-bromo-1-methoxy-2-Naphthalenecarboxaldehyde
https://huagongshe.com/de/reaction/550239
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | 2,4-Dibromo-1-methoxynaphthalene | HCID 3572059 | — |
| Edukt | HCID 178418244 | HCID 178418244 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 4-bromo-1-methoxy-2-Naphthalenecarboxaldehyde | HCID 86221944 | 15,1% |
Reaktionsschritte
In a nitrogen stream, an n-butyllithium hexane solution (1.6 M, 56.9 ml, 91.1 mmol) was added dropwise to a solution of 2,4-dibromo-1-methoxy-naphthalene (30.3 g, 95.9 mmol) in THF (1,800 ml) at −78° C. and the reaction mixture was stirred at the same temperature for 30 minutes. To this mixture, N,N-dimethylformamide (8.9 ml, 115.1 mmol) was added at −78° C. The mixture was stirred at the same temperature for three hours, and then a saturated ammonium chloride aqueous solution was added thereto and the mixture was extracted with ether. The organic layer was washed with a saturated sodium chloride aqueous solution and dried (anhydrous magnesium sulfate), and then the solvent was distilled under reduced pressure. The obtained residue was purified by silica gel column chromatography [developing solution=ethyl acetate:n-hexane (1:8)] to obtain the title compound (3.85 g, 15%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07943748B2 |
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| Quelldatensatz | uspto-grants-2011_05 |
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| ORD ID | ord-d1582ed2dc19494f88b89f6228af3535 |
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| Quellennotiz | uspto-grants-2011_05 |
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