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HRID 1830724생성일: 2026년 10월 26일

Benzaldehyde → N-benzylpiperidine-4-carboxamide

https://huagongshe.com/reaction/1830724

반응식

참여 물질

역할이름HCID투입량
반응물BenzaldehydeHCID 240—
반응물4-PiperidinecarboxamideHCID 3772—
반응물Sodium triacetoxyborohydrideHCID 5049666—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물N-benzylpiperidine-4-carboxamideHCID 386806451.7%

반응 단계

To a suspension of isonipecotamide (12.3 g, 96 mmol) in 200 mL of dichloromethane, was added, benzaldehyde (10.6 g, 100 mmol) and sodium triacetoxyborohydride (29.7 gm, 140 mmol) and the mixture was stirred at room temperature for 5 days. The thick white mixture was diluted with 100 mL water and extracted with EtOAc (2×20 mL). The aqueous phase was basified with 1N NaOH to pH>12. The resulting white precipitate was collected by suction filtration. The white solid was subsequently taken up in 50 mL of EtOAc, and was washed with 20 mL of brine, then dried (MgSO4), filtered and concentrated to give 10.84 g (50%) of the desired product. 1H-NMR (400 MHz, CDCl3) δ7.85 (m, 5H), 5.45 (s, 1H), 5.34 (s, 1H), 3.5 (s, 2H), 2.93 (d, J=10.96 Hz, 2H), 2.16 (t, J=12.13 Hz, 1H), 2.01 (t, J=11.74 Hz, 2H), 1.87 (d, J=12.52 Hz, 2H), 1.76 (q, J=12.52 Hz, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07067506B2
출처 데이터셋uspto-grants-2006_06
ORD IDord-b6e5831158794da89645e89ab4cd8afb
출처 메모uspto-grants-2006_06