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HRID 1661866作成日:2026年10月25日

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

https://huagongshe.com/reaction/1661866

反応式

関与物質

役割名称HCID仕込み量
反応物N-(5-Carboxypentyl)maleamic acidHCID 329056—
反応物Sodium AcetateHCID 517045—
溶媒Acetic AnhydrideHCID 7918—
生成物6-Maleimidohexanoic acidHCID 573683—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08030459B2
出典データセットuspto-grants-2011_10
ORD IDord-2c1698d60ba24d6c979635b6666a6793
出典メモuspto-grants-2011_10