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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 459724생성일: 2026년 10월 25일

Formaldehyde → 1-Methylpiperidine-4-carboxamide

https://huagongshe.com/reaction/459724

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물4-PiperidinecarboxamideHCID 3772—
촉매PalladiumHCID 23938—
용매WaterHCID 962—
생성물1-Methylpiperidine-4-carboxamideHCID 33901164.5%

반응 단계

Isonipecotamide (10 g, 78.0 mmoles) was dissolved in distilled water (100 mL) and 37% aqueous formaldehyde (7.6 mL, equivalent to 2.81 g HCHO, 93.6 mmoles) was added. Wet 10% Pd—C (8 spoon spatulas) was added under argon and the mixture was hydrogenated at 25° C. and 50 psi for 43 h. The catalyst was filtered off through Celite and the latter was washed with water and methanol. The combined filtrates were evaporated to dryness and the residue was chromatographed on a silica gel column (60×5 cm) using 8%–10%–20% (10% conc. ammonium hydroxide in methanol)-dichloromethane as the eluant to give 1-methylisonipecotamide (7.15 g, 64%): FABMS: m/z 143.1 (MH+); HRFABMS: m/z 143.1184 (MH+). Calcd. for C7H15N2O: m/z 143.1184; δH (d6-DMSO) 1.50/1.57 (4H, m, CH2), 1.76/1.94 (4H, m, CH2), 2.10 (3H, s, —NCH3), 2.72 (1H, m, CH) and 6.68/7.18 ppm (2H, m, CONH2); δC (d6-DMSO)CH3: 41.2; CH2: 28.5, 28.5, 54.9, 54.9; CH: 46.2; C: 176.7.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07196078B2
출처 데이터셋uspto-grants-2007_03
ORD IDord-967c34a506014927805b854263b564a2
출처 메모uspto-grants-2007_03