162358-05-6

基本信息
4-十二烷基苯乙醇
2-(4-正辛基苯)乙醇
乙酸-[2-(4-辛基苯基)]乙醇
Benzeneethanol, 4-octyl
4-Octylphenethyl alcohol
2-(4-OCTYLPHENYL)ETHANOL
物理化學(xué)性質(zhì)
制備方法
![乙酸-[2-(4-辛基苯基)]乙酯](/CAS/GIF/162358-04-5.gif)
162358-04-5
![乙酸-[2-(4-辛基苯基)]乙醇](/StructureFile/ChemBookStructure20/GIF/CB0507640.gif)
162358-05-6
以乙酸-[2-(4-辛基苯基)]乙酯為原料合成4-十二烷基苯乙醇的一般步驟如下:向4-辛基苯乙酸乙酯(500 mg,1.81 mmol)的甲醇(MeOH,10 mL)溶液中加入甲醇鈉(195 mg,3.61 mmol)。將反應(yīng)混合物加熱回流6小時(shí)。反應(yīng)完成后,蒸發(fā)溶劑,并將殘余物在乙酸乙酯(EtOAc)和水之間分配。分離有機(jī)層,用飽和食鹽水(brine)洗滌。有機(jī)相用無水硫酸鈉(Na2SO4)干燥,過濾后蒸發(fā)溶劑,得到4-辛基苯乙醇(390 mg,收率92%),為黃色油狀物。產(chǎn)物經(jīng)1H NMR(400 MHz,CDCl3)表征:δ 0.88(t,J = 6.8 Hz,3H),1.22-1.30(m,10H),1.55-1.63(m,2H),2.57(t,J = 7.8 Hz,2H),2.83(t,J = 6.6 Hz,2H),3.84(t,J = 6.6 Hz,2H),7.11(s,4H)。
參考文獻(xiàn):
[1] Journal of Organic Chemistry, 2004, vol. 69, # 11, p. 3950 - 3952
[2] Chemical Communications, 2013, vol. 49, # 21, p. 2136 - 2138
[3] Patent: WO2014/118556, 2014, A2. Location in patent: Page/Page column 50
[4] Journal of Medicinal Chemistry, 2000, vol. 43, # 15, p. 2946 - 2961
[5] Patent: US2014/235895, 2014, A1. Location in patent: Paragraph 0253