戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 279351作成日:2026年10月25日

1-Chloro-4-(chloromethyl)benzene → 3-Amino-1-(4-chlorobenzyl)homopiperidine

https://huagongshe.com/reaction/279351

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Potassium CarbonateHCID 11430—
反応物Azepan-3-amineHCID 2756445—
溶媒AcetonitrileHCID 6342—
生成物3-Amino-1-(4-chlorobenzyl)homopiperidineHCID 1842623993%

反応条件

温度70 °C

反応手順

A solution of 3-aminohomopiperidine (1.71 g, 15 mmol) in CH3CN (45 mL) was treated with p-chlorobenzyl chloride (463 mg, 2.9 mmol) and K2CO3 (828 g, 6 mmol) and heated to 70° C. for 9 h. The reaction mixture was cooled to 25° C. and concentrated to afford a yellow solid. The residue was partitioned between H2O (5 mL) and EtOAc (50 mL), and extracted with EtOAc (2×50 mL). The combined organic extracts were washed with brine (20 mL), dried (Na2SO4) and concentrated. The resulting yellow oil was purified by chromatography (SiO2, 5-20% CH3OH—CH2Cl2 gradient elution) to afford the desired product as a yellow oil (639 mg, 93%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06362177B1
出典データセットuspto-grants-2002_03
ORD IDord-008f99bd4ef24cc2a51d056e6de3a40f
出典メモuspto-grants-2002_03