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HRID 599357作成日:2026年10月26日

Iodine → 6,7-Dichloro-4-formylquinoline

https://huagongshe.com/reaction/599357

反応式

関与物質

役割名称HCID仕込み量
反応物IodineHCID 807—
反応物Trifluoroacetic acidHCID 6422—
反応物2-Iodo-2-methylpropaneHCID 11206—
反応物Sodium ThiosulfateHCID 24477—
反応物Sodium BicarbonateHCID 516892—
反応物6,7-Dichloro-4-methylquinolineHCID 21992880—
触媒Ferrous chloride tetrahydrateHCID 16211588—
溶媒Dimethyl SulfoxideHCID 679—
溶媒Ethyl AcetateHCID 8857—
生成物6,7-Dichloro-4-formylquinolineHCID 8661800599%

反応手順

Trifluoroacetic acid (360 μL, 4.7 mmol), tert-butyl iodide (450 μL, 3.8 mmol), iodine (990 mg, 3.9 mmol) and iron(II) chloride tetrahydrate (170 mg, 0.85 mmol) were added sequentially to a solution of 6,7-dichloro-4-methylquinoline (Reference compound No. 1-2, 790 mg, 3.7 mmol) in dimethylsulfoxide (18 mL) at room temperature, and the mixture was stirred at 80° C. for 7 hours. Then saturated sodium thiosulfate aqueous solution (100 mL) was added, and then ethyl acetate (300 mL) and saturated aqueous sodium hydrogencarbonate solution (200 mL) were added thereto. The mixture was separated into the organic layer and the aqueous layer, and the organic layer was washed with saturated brine (100 mL), dried over anhydrous magnesium sulfate, The solvent was evaporated under reduced pressure to give 840 mg of the title reference compound as a brown solid (Yield: 99%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07897774B2
出典データセットuspto-grants-2011_03
ORD IDord-ef43c900f8c9448a885bb5d4533180fa
出典メモuspto-grants-2011_03