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HRID 1661866생성일: 2026년 10월 24일

N-(5-Carboxypentyl)maleamic acid → 6-Maleimidohexanoic acid

https://huagongshe.com/ko/reaction/1661866

반응식

참여 물질

역할이름HCID투입량
반응물N-(5-Carboxypentyl)maleamic acidHCID 329056—
반응물Sodium AcetateHCID 517045—
용매Acetic AnhydrideHCID 7918—
생성물6-Maleimidohexanoic acidHCID 573683—

반응 단계

The acid 14 (4.5 g, 21 mmol) was refluxed in 60 mL of (Ac)2O with NaOAc (1.72 g, 21 mmol) for 3 h. After cooling, the reaction mixture was concentrated. The residue was dissolved in EtOAc, washed with brine, dried over MgSO4, filtered and evaporated to give a deep red oil that was purified by silica gel column chromatography (CHCl3:MeOH/99:1). The maleimide product 15 was isolated as a white solid (1.4 g, 32%). 1H NMR (DMSO-d6): δ 1.18-1.24 (2H, m), 1.45-1.52 (4H, m), 2.18 (2H, t, J=7.5), 3.38 (2H, t, J=7.0), 7.01 (2H, s).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08030459B2
출처 데이터셋uspto-grants-2011_10
ORD IDord-2c1698d60ba24d6c979635b6666a6793
출처 메모uspto-grants-2011_10