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HRID 6813作成日:2026年10月23日

Sodium Cyanide → 2-Oxo-1,2,3,4-tetrahydroquinoline-6-carbonitrile

https://huagongshe.com/ja/reaction/6813

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CyanideHCID 8929—
反応物6-Iodo-3,4-dihydroquinolin-2(1H)-oneHCID 22018951—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
触媒HCID 178418397HCID 178418397—
生成物2-Oxo-1,2,3,4-tetrahydroquinoline-6-carbonitrileHCID 15270576—

反応手順

6-Iodo-3,4-dihydroquinolin-2(1H)-one (1.50 g; 5.50 mmol), sodium cyanide (0.54 g; 11.0 mmol), copper (I) iodide (0.105 g; 0.5 mmol) and tetrakis(triphenylphosphine)palladium(0) (0.32 g; 0.3 mmol) were combined in a flask equipped with a reflux condenser. The flask was subjected to several evacuation-nitrogen purge cycles followed by the addition of acetonitrile (25 mL). The reaction was heated to reflux for 5 hours. After cooling, the reaction was diluted with ethyl acetate (200 mL), filtered through CELITE diatomaceous earth and rinsed with copious amounts of ethyl acetate. The organic solution was washed twice with brine (50 mL), dried over sodium sulfate, filtered through a fritted funnel, and the volatiles were removed under vacuum. The crude residue was crystallized from methanol, which afforded the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07084156B2
出典データセットuspto-grants-2006_08
ORD IDord-dc386eeb65804bc3a3674cae524f7269
出典メモuspto-grants-2006_08