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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2213785Generated: October 26, 2026

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

https://huagongshe.com/reaction/2213785

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantAcetonitrileHCID 6342—
ReactantButyllithiumHCID 178418339—
ReactantHCID 178496951HCID 178496951—
SolventTetrahydrofuranHCID 8028—
Product7-Methoxy-4-oxo-1,4-dihydrobenzo[g]quinoline-3-carbonitrileHCID 9813663—

Reaction Conditions

Temperature-78 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07105531B2
Source datasetuspto-grants-2006_09
ORD IDord-44e212385697476eaac688ef198c6546
Source noteuspto-grants-2006_09