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HRID 1972102作成日:2026年10月26日

Hydrochloric Acid → 8-Methoxy-1,2,3,4-tetrahydroquinoline

https://huagongshe.com/reaction/1972102

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Ammonium HydroxideHCID 14923—
反応物8-MethoxyquinolineHCID 70310—
反応物Sodium cyanoborohydrideHCID 5003444—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
生成物8-Methoxy-1,2,3,4-tetrahydroquinolineHCID 520034582%

反応条件

温度0 °C

反応手順

Add sodium cyanoborohydride (505 g, 8.11 mol) in EtOH (1 L) to a solution of 8-methoxy quinoline (425 g, 2.673 mol) in EtOH (9 L), and stir. Cool the reaction mixture to an internal temperature of 0° C. and add HCl (35%, 1.12 L, 10.962 mol) dropwise over 60 min so that the internal temperature did not rise above 20° C. Allow the reaction mixture to warm to ambient temperature and then heat to reflux for 2.5 hours. Cool to ambient temperature and stir overnight. Add ammonium hydroxide (25%, 1 L); dilute with water (15 L); and extract the mixture with dichloromethane (3×10 L). Combine the organic layers and dry over sodium sulfate. Remove the solids by filtration. Collect the filtrate and concentrate under reduced pressure to give a residue. Purify the residue by silica gel flash chromatography, eluting with ethyl acetate: hexane (1:10) to give the title compound (357 g, 82%). ESI (m/z) 164(M+H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08431706B2
出典データセットuspto-grants-2013_04
ORD IDord-0c60f68931f74060a2c62cad70cdb324
出典メモuspto-grants-2013_04