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HRID 1036857作成日:2026年10月25日

4-Chloroaniline → 2-(3-Bromophenyl)-6-chloro-4,4-dimethyl-1,2,3,4-tetrahydroquinoline

https://huagongshe.com/reaction/1036857

反応式

関与物質

役割名称HCID仕込み量
反応物4-ChloroanilineHCID 7812—
反応物IsobutyleneHCID 8255—
反応物3-BromobenzaldehydeHCID 76583—
反応物Ytterbium triflateHCID 2733225—
溶媒AcetonitrileHCID 6342—
溶媒Ethyl AcetateHCID 8857—
生成物2-(3-Bromophenyl)-6-chloro-4,4-dimethyl-1,2,3,4-tetrahydroquinolineHCID 6729125940%

反応条件

温度85 °C

反応手順

To a stirred solution of 4-chlorophenylamine (10.0 g, 78.4 mmol) and 3-bromobenzaldehyde (9.2 mL, 78.4 mmol) in acetonitrile (150 mL) were added isobutene (21.0 mL, 313.5 mmol) and ytterbium(III) trifluoromethanesulfonate (Yb(OTf)3) (5.8 g, 9.5 mmol). The resulting mixture was stirred at 85° C. for 18 h in sealed tube. The mixture was diluted with ethyl acetate (300 mL) and washed with water (100 mL×2) and brine (100 mL×2) and then dried over anhydrous sodium sulfate. The solvent was removed in vacuo and the residue was purified by ISCO combi-flash chromatography (gradient elution, 0-10% ethyl acetate in petroleum ether) to afford 2-(3-bromo-phenyl)-6-chloro-4,4-dimethyl-1,2,3,4-tetrahydro-quinoline (11.0 g, 40.0%) as a light yellow solid: LC/MS m/e obsd. (ESI+) [(M+H)+] 350.0 & 352.0.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08546427B2
出典データセットuspto-grants-2013_10
ORD IDord-09c2f1c3d63145a3be379713e6a58b08
出典メモuspto-grants-2013_10