518044-32-1 丙酸叔丁酯-四聚乙二醇
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安全说明
WGK Germany:WGK 3 海关编码:2918999090 存储类别:10 - 可燃性液体
用途与制备
医药
112-60-7 1663-39-4 518044-32-1 一般步骤:向三缩四乙二醇(40.61 mL; 45.64 g; 235 mmol)的无水四氢呋喃(THF,125 mL)溶液中加入一片钠(约1/4 cm)。待钠完全反应后,在20分钟内逐滴加入丙烯酸叔丁酯(11.98 mL; 10.57 g; 82.5 mmol),并将反应混合物在室温下搅拌过夜。反应完成后,用1N NaOH溶液调节pH至7-8,随后在减压下除去溶剂。将残余物溶解于饱和NaHCO3和NaCl混合溶液(75 mL)中,并用乙酸乙酯(EtOAc,3×100 mL)萃取。合并有机层,用无水硫酸镁(MgSO4)干燥,过滤后减压蒸发溶剂,得到叔丁基-15-羟基-4,7,10,13-四氧杂十五烷酸酯(21.87 g; 67.8 mmol; 产率82%,基于丙烯酸叔丁酯计算),为无色油状物。产物经1H-NMR(500 MHz, CDCl3, TMS)和13C{1H}-NMR(126 MHz, CDCl3, TMS)表征,数据如下:1H-NMR δ [ppm] = 3.77-3.57 (m, 18H, OCH2); 3.01 (bs, 1H, OH); 2.51 (t, 2H, J = 6.6 Hz, CH2COO'Bu); 1.45 (s, 9H, C(CH3)3); 13C{1H}-NMR δ [ppm] = 171.1 (COO); 80.7 (C(CH3)3); 72.6 / 70.8 / 70.7 / 70.6 / 70.5 / 67.0 (OCH2); 61.9 (HOCH2); 36.4 (CH2CO); 28.2 (C(CH3)3)。 参考文献: [1] Synthetic Communications, 2004, vol. 34, # 13, p. 2425 - 2432 [2] Patent: WO2016/146638, 2016, A1. Location in patent: Page/Page column 20 [3] Patent: WO2017/147542, 2017, A2. Location in patent: Paragraph 00162 [4] Patent: WO2018/89373, 2018, A2. Location in patent: Paragraph 0638-0639 [5] Tetrahedron, 2011, vol. 67, # 12, p. 2251 - 2259