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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktLithium HexamethyldisilazideHCID 2733832—
Edukt3,5-Dichloro-4-methylpyridineHCID 10953827—
Edukt4-Methoxy-8-nitro-dibenzofuran-1-carbonyl chlorideHCID 86005858—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-(3,5-Dichloro-pyridin-4-yl)-1-(4-methoxy-8-nitro-dibenzo-furan-1-yl)-ethanoneHCID 6714829632,3%

Reaktionsbedingungen

Temperatur-60 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07968724B2
Quelldatensatzuspto-grants-2011_06
ORD IDord-0f7d5c369b52429c9bd9f24cb6b21a6e
Quellennotizuspto-grants-2011_06