1585-90-6

基本信息
馬來酰亞胺-一聚乙二醇
N-(2-羥乙基)馬來酰亞胺
N-(2-羥乙基)馬來酰亞胺
1-(2-羥乙基)-1H-吡咯-2,5-二酮
N-(Ethanol)maleimide
N-Hydroxyethyl MaleiMide
N-hydroxyethylMaleiciMide
N-(2-HYDROXYETHYL)MALEIMIDE
1-(2-Hydroxyethyl)maleimide
N-(2-Hydroxyethyl)MaleiMide,99%
N-(2-Hydroxyethyl)MaleiMide 97%
1-(2-HYDROXY-ETHYL)-PYRROLE-2,5-DIONE
1-(2-hydroxyethyl)-1H-pyrrole-2,5-dione
物理化學(xué)性質(zhì)
制備方法
![4-(2-羥基乙基)-10-噁-4-氮雜三環(huán)[5.2.1.02,6]-8-癸烯-3,5-二酮](/CAS/GIF/32620-90-9.gif)
32620-90-9

1585-90-6
以3a,4,7,7a-四氫-2-(2'-羥乙基)-4,7-環(huán)氧-1H-異吲哚-1,3(2H)-二酮(HEMI-A)為原料合成N-(2-羥乙基)馬來酰亞胺(HEMI)的一般步驟:將0.19 mol(40 g)HEMI-A與227 g二甲苯和0.005 g甲基氫醌(MEHQ,作為抗氧化劑)混合。在氮氣保護下,于130℃回流加熱3小時15分鐘,使HEMI-A轉(zhuǎn)化為HEMI,轉(zhuǎn)化率達98.7%,反應(yīng)產(chǎn)率約為98.7%。反應(yīng)完成后,將反應(yīng)器冷卻至室溫,過濾反應(yīng)混合物,并用15 g二甲苯洗滌固體產(chǎn)物。將洗滌后的固體在真空下干燥,得到25.1 g HEMI,基于HEMI-A的產(chǎn)率為93%。通過1H-NMR分析確認(rèn)HEMI的純度大于99%。合并母液和洗液,測定總質(zhì)量為230.2 g,其中含有1.17 g HEMI,可按上述方法回收或循環(huán)利用。
參考文獻:
[1] Patent: WO2007/44169, 2007, A1. Location in patent: Page/Page column 10
[2] Dyes and Pigments, 2017, vol. 145, p. 518 - 527
[3] Organic Letters, 2011, vol. 13, # 16, p. 4364 - 4367
[4] Advanced Functional Materials, 2014, vol. 24, # 33, p. 5261 - 5268,8
[5] Journal of Controlled Release, 2018, vol. 285, p. 187 - 199