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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2213785Erstellt: 27. Oktober 2026

Acetic Acid → 7-Methoxy-4-oxo-1,4-dihydrobenzo[g]quinoline-3-carbonitrile

https://huagongshe.com/reaction/2213785

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktAcetonitrileHCID 6342—
EduktButyllithiumHCID 178418339—
EduktHCID 178496951HCID 178496951—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt7-Methoxy-4-oxo-1,4-dihydrobenzo[g]quinoline-3-carbonitrileHCID 9813663—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

To a solution of 4.75 mL (11.88 mmol) of n-butyllithium (2.5M in hexane) in 4.0 mL of tetrahydrofuran at −78° C. is added dropwise a solution of 0.68 mL (13.1 mmol) of acetonitrile in 6.8 mL of tetrahydrofuran. After completion of addition, the suspension is stirred for 10 minutes. To this is added 1.36 g (4.75 mmol) of methyl 3-{[(E)-(dimethylamino)methylidene]amino}-7-methoxy-2-naphthoate in 32 mL of tetrahydrofuran dropwise. The resulting reaction mixture is stirred at −78° C. for 1 hour, at −5° C. for 1 hour and at room temperature for 15 minutes. The reaction mixture is again cooled to −78° C. and 1.72 g (28.6 mmol) of acetic acid is added dropwise. After addition of the acetic acid, the reaction mixture is allowed to warm to room temperature. The precipitate is collected by filtration and washed sequentially with water, acetonitrile and methanol. After drying in vacuo, this yields 796.9 mg (67%) of 7-methoxy-4-oxo-1,4-dihydrobenzo[g]quinoline-3-carbonitrile as a deep yellow solid, mp>260° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07105531B2
Quelldatensatzuspto-grants-2006_09
ORD IDord-44e212385697476eaac688ef198c6546
Quellennotizuspto-grants-2006_09