74733-29-2
74733-29-2 結(jié)構(gòu)式
基本信息
2-Fluoro-4-Methyl-benzoic acid Methyl ester
物理化學(xué)性質(zhì)
制備方法
67-56-1
7697-23-6
74733-29-2
(f)2-氟-4-甲基苯甲酸甲酯(5):方法A:在攪拌下,將2-氟-4-甲基苯甲酸(2.0g,13.0mmol)和K2CO3(3.6g,26.0mmol)的乙腈(15mL)混合物中逐滴加入CH3I(1.6mL,25.6mmol)。反應(yīng)混合物加熱回流過夜后,減壓蒸餾除去溶劑。殘余物用EtOAc溶解,依次用水和飽和食鹽水洗滌,無水Na2SO4干燥,過濾后減壓濃縮。粗產(chǎn)物通過硅膠柱色譜純化,洗脫劑為己烷/EtOAc(6:1),得到白色固體5(1.73g,收率79%),熔點51-53℃。1H NMR(CDCl3)δ:7.83(t,J=8.0Hz,1H),7.00(dd,J=8.0,1.0Hz,1H),6.95(d,J=12.0Hz,1H),3.91(s,3H),2.39(s,3H)。方法B:在攪拌下,將2-氟-4-甲基苯甲酸(7.0g,45.4mmol)的MeOH(100mL)溶液中逐滴加入濃硫酸(5mL)。反應(yīng)混合物加熱回流過夜后,減壓蒸餾除去溶劑。殘余物用EtOAc溶解,依次用飽和NaHCO3水溶液和飽和食鹽水洗滌,無水Na2SO4干燥,過濾后減壓濃縮。粗產(chǎn)物通過硅膠柱色譜純化,洗脫劑為己烷/EtOAc(6:1),得到白色固體5(6.88g,收率90%)。分析數(shù)據(jù)與方法A相同。
參考文獻:
[1] Patent: WO2010/116270, 2010, A1. Location in patent: Page/Page column 55
[2] Organic Process Research and Development, 2011, vol. 15, # 3, p. 565 - 569
[3] Bioorganic and Medicinal Chemistry Letters, 2014, vol. 24, # 7, p. 1742 - 1747
[4] Bioorganic and Medicinal Chemistry Letters, 2015, vol. 24, # 7, p. 1742 - 1747
[5] Patent: EP1449844, 2004, A1. Location in patent: Page 22
