91407-41-9

制备方法

91407-40-8

91407-41-9
以5-氟-2-羟基苯甲醛肟(920 mg,5.93 mmol)为原料,将其溶解于乙酸酐(15 mL)中。随后,向该混合物中加入由KOH(2 g)溶于H2O(10 mL)和乙醇(10 mL)的溶液。将反应混合物在80℃下加热2小时,之后冷却至室温。用6N HCl调节反应液的pH至7,然后用异丙醇/二氯甲烷(1:3,v/v)混合溶剂萃取两次。合并有机层,并用无水硫酸钠干燥。通过硅胶柱色谱法,使用己烷/乙酸乙酯(5:1,v/v)作为洗脱剂,对所得残余物进行纯化,得到目标产物2-羟基-5-氟苯腈(800 mg,收率100%)。质谱(DCI/NH3)显示m/z 136(M + 1)+。1H NMR(500 MHz,DMSO-d6)δ ppm:6.99(dd,J = 9.05, 4.37 Hz,1H),7.36(td,J = 9.05, 3.12 Hz,1H),7.53(dd,J = 8.42, 3.43 Hz,1H),11.04(m,1H)。
参考文献:
[1] Patent: WO2005/111003, 2005, A1. Location in patent: Page/Page column 131
[2] Patent: EP2258697, 2010, A1. Location in patent: Page/Page column 40
[3] Patent: CN107778216, 2018, A. Location in patent: Paragraph 0023; 0024
[4] Patent: CN107778215, 2018, A. Location in patent: Paragraph 0023; 0024