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HRID 862561作成日:2026年10月27日

Imidazole → 2-Cyanomethyl-1,2,3,4-tetrahydroquinoline

https://huagongshe.com/reaction/862561

反応式

関与物質

役割名称HCID仕込み量
反応物ImidazoleHCID 795—
反応物IodineHCID 807—
反応物Sodium CyanideHCID 8929—
反応物TriphenylphosphineHCID 11776—
反応物Sodium ThiosulfateHCID 24477—
反応物(1,2,3,4-Tetrahydroquinolin-2-yl)methanolHCID 15052240—
溶媒Acetonitrile tolueneHCID 21584213—
生成物2-Cyanomethyl-1,2,3,4-tetrahydroquinolineHCID 58341994%

反応条件

温度0 °C

反応手順

To a solution of 2-hydroxymethyltetrahydroquinoline (35.9 g, 0.22 mol), imidazole (35.95 g, 0.528 mol), and triphenylphosphine (69.24 g, 0.264 mol) in a mixed solvent of 5:1 toluene/acetonitrile (750 mL) was added iodine (61.42 g, 0.242 mol) at 0° C. The mixture was stirred for 15 min at 0° C. and for 30 min at room temperature. Aqueous sodium thiosulfate solution (200 mL) was added. The organic layer was separated, washed with brine, dried over magnesium sulfate, and concentrated. The residue was triturated with diethyl ether and the insoluble materials were removed by filtration. The filtrate was concentrated and the residual oil was dissolved in DMF (200 mL). To the solution was added sodium cyanide (43.2 g, 0.881 mol) and the mixture was heated at 80° C. for 10 h. The resulting mixture was poured into ice-water and extracted with a mixture of toluene and ethyl acetate. The organic layer was washed with brine, dried over magnesium sulfate, and concentrated. The residue was purified by silica gel column chromatography with 1:1 hexane/dichloromethane to 100% dichloromethane as eluents to give 31.6 g of the title compound (94%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05719152
出典データセットuspto-grants-1998_02
ORD IDord-b02b8705a4b848629461a5fc303bd891
出典メモuspto-grants-1998_02