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HRID 133583作成日:2026年10月26日

1-Chloro-4-(chloromethyl)benzene → 3-Carbamoyl-1-(4-chlorobenzyl)piperidine

https://huagongshe.com/reaction/133583

反応式

関与物質

役割名称HCID仕込み量
反応物1-Chloro-4-(chloromethyl)benzeneHCID 7723—
反応物TriethylamineHCID 8471—
反応物3-PiperidinecarboxamideHCID 92980—
反応物Sodium BicarbonateHCID 516892—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
溶媒AcetonitrileHCID 6342—
生成物3-Carbamoyl-1-(4-chlorobenzyl)piperidineHCID 284579755.2%

反応条件

温度50 °C

反応手順

Triethylamine (7.0 mL, 50 mmol) and 4-chlorobenzyl chloride (8.05 g, 50 mmol) were added to a solution of nipecotamide (6.40 g, 50 mmol) in acetonitrile (150 mL) and ethanol (20 mL). The resulting reaction mixture was stirred at 50° C. for 16 hours and cooled to room temperature. A saturated aqueous solution of NaHCO3 (50 mL) and water (150 mL) were then added, and the resulting mixture was extracted with ethyl acetate (150 mL×3). The extracts were washed with brine, dried over Na2SO4 and concentrated to afford a light-red solid. The obtained crude solid was washed with ether (100 mL) to provide 3-carbamoyl-1-(4-chlorobenzyl)piperidine (6.98 g, 54%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07390830B1
出典データセットuspto-grants-2008_06
ORD IDord-6f4b2841fe374baeadbc5ec0cd15c8f0
出典メモuspto-grants-2008_06