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HRID 1804588생성일: 2026년 10월 27일

2-Acetyl-6-methylpyridine → 1-(6-Methylpyridin-2-yl)ethan-1-amine

https://huagongshe.com/reaction/1804588

반응식

참여 물질

역할이름HCID투입량
반응물2-Acetyl-6-methylpyridineHCID 138872—
반응물Ammonium AcetateHCID 517165—
반응물Sodium cyanoborohydrideHCID 5003444—
용매MethanolHCID 887—
생성물1-(6-Methylpyridin-2-yl)ethan-1-amineHCID 232201245%

반응 단계

To a solution of 2-acetyl-6-methylpyridine (4.7 g, 34.8 mmol) in anhydrous methanol (100 ml) was added ammonium acetate (26.8 g, 348 mmol) and sodium cyanoborohydride (1.75 g, 27.8 mmol) and the resulting mixture stirred at RT overnight. The mixture was evaporated and the residue dissolved in water and basified by the addition of KOH and extracted with DCM (×3). The DCM layers were combined and washed with sat. NaCl, dried over MgSO4, filtered and evaporated. The residue was purified by column chromatography on silica to afford the title compound (i-14) (eluent: 5% MeOH in DCM) to give 2.8 g (59%) as a clear oil. 1H NMR (CDCl3): 1.41 (d, J 6.7 Hz, 3H), 1.78 (brs, 2H), 2.54 (s, 3H), 4.21 (q, J 6.7 Hz, 1H), 6.99 (d, J 7.6 Hz, 1H), 7.09 (d, J 7.7 Hz, 1H), 7.52 (m, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08354403B2
출처 데이터셋uspto-grants-2013_01
ORD IDord-aa7429a9a02f43bcbf8a180f34a55ddf
출처 메모uspto-grants-2013_01