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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1280990생성일: 2026년 10월 25일

Hydrochloric Acid → 3-Aminomethyl-1-(p-chlorobenzyl)piperidine

https://huagongshe.com/reaction/1280990

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물Sodium HydroxideHCID 14798—
반응물Borane;tetrahydrofuranHCID 2723981—
반응물3-Carbamoyl-1-(4-chlorobenzyl)piperidineHCID 2845797—
용매TetrahydrofuranHCID 8028—
생성물3-Aminomethyl-1-(p-chlorobenzyl)piperidineHCID 1842622257.2%

반응 조건

온도70 °C

반응 단계

3-Carbamoyl-1-(4-chlorobenzyl)piperidine (3.80 g, 15 mmol) was dissolved in THF (30 mL) and 1 M BH3-THF (9.4 mL) was added to the solution. The reaction mixture was stirred at 70° C. for 15 h. After the mixture was cooled to 0° C., 2 N aqueous HCl solution (50 mL) was added and the mixture was stirred at room temperature for additional 3 h, basicified with 4 N aqueous NaOH solution, and extracted with ethyl acetate (100 mL×3). The combined extracts were washed with brine, dried over anhydrous Na2SO4, filtered and concentrated. Column chromatography (SiO2, ethyl acetate/EtOH/Et3N=80/15/5) afforded 3-(aminomethyl)-1-(4-chlorobenzyl)piperidine (2.05 g, 55%): 1H NMR (CDCl3, 400 MHz) δ1.00-1.09 (m, 1 H), 1.50-1.87 (m, 7 H), 1.97-2.06 (m, 1 H), 2.65-2.77 (m, 2 H), 3.16-3.26 (m, 2 H), 3.32 (s, 2 H), 3.40. (d, J=13.3 Hz, 1 H), 3.49 (d, J=13.3 Hz, 1 H), 7.22-7.33 (m, 5 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06451842B1
출처 데이터셋uspto-grants-2002_09
ORD IDord-f2c903188bf04f81a91f387cc864b29f
출처 메모uspto-grants-2002_09