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HRID 279351생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/279351

반응식

참여 물질

역할이름HCID투입량
반응물1-Chloro-4-(chloromethyl)benzeneHCID 7723—
반응물Potassium CarbonateHCID 11430—
반응물Azepan-3-amineHCID 2756445—
용매AcetonitrileHCID 6342—
생성물3-Amino-1-(4-chlorobenzyl)homopiperidineHCID 1842623993%

반응 조건

온도70 °C

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06362177B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-008f99bd4ef24cc2a51d056e6de3a40f
출처 메모uspto-grants-2002_03