HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2427857Erstellt: 27. Oktober 2026
Lithium Hexamethyldisilazide → 2-(3,5-Dichloro-pyridin-4-yl)-1-(4-methoxy-8-nitro-dibenzo-furan-1-yl)-ethanone
https://huagongshe.com/reaction/2427857
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Edukt | 3,5-Dichloro-4-methylpyridine | HCID 10953827 | — |
| Edukt | 4-Methoxy-8-nitro-dibenzofuran-1-carbonyl chloride | HCID 86005858 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 2-(3,5-Dichloro-pyridin-4-yl)-1-(4-methoxy-8-nitro-dibenzo-furan-1-yl)-ethanone | HCID 67148296 | 32,3% |
Reaktionsschritte
A solution of 3,5-dichloro-4-methyl-pyridine (0.593 g, 3.66 mmoles) in tetrahydrofuran (200 mL) is cooled to −60° C. under nitrogen atmosphere. A 1M solution of lithium bis(trimethylsilyl) amide (4.4 mL, 4.4 mmoles) is added dropwise and the resulting mixture is stirred at −60° C. for 30 minutes. A solution of 4-methoxy-8-nitro-dibenzofuran-1-carbonyl chloride (3a) (0.75 g, 2.44 mmoles) in dry tetrahydrofuran (20 mL) is added dropwise, maintaining the temperature below −60° C. After stirring for 15 minutes at −60° C., the mixture is stirred at room temperature for 3.5 hours. The mixture is then quenched with a saturated NH4Cl solution (20 mL); the product precipitated as a solid which is recovered by filtration and washed with methanol to yield 340 mg of the title compound.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07968724B2 |
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| Quelldatensatz | uspto-grants-2011_06 |
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| ORD ID | ord-0f7d5c369b52429c9bd9f24cb6b21a6e |
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| Quellennotiz | uspto-grants-2011_06 |
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