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HRID 228564生成日期:2026年10月24日

聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯] → 1-{2-[(6,7-Dimethoxy-4-quinolyl)oxy]-5-iodophenyl}-1-propanol

https://huagongshe.com/zh-CN/reaction/228564

反应方程式

参与物

角色名称HCID投料
反应物聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯]HCID 962—
反应物2-[(6,7-Dimethoxy-4-quinolyl)oxy]-5-iodobenzaldehydeHCID 23078419—
反应物HCID 178418443HCID 178418443—
溶剂四氢呋喃HCID 8028—
产物1-{2-[(6,7-Dimethoxy-4-quinolyl)oxy]-5-iodophenyl}-1-propanolHCID 68832550—

反应条件

温度0 °C

反应步骤

2-[(6,7-Dimethoxy-4-quinolyl)oxy]-5-iodobenzaldehyde was dissolved in anhydrous tetrahydrofuran (1 ml) to prepare a solution. A 1 M tetrahydrofuran solution (0.5 ml) of ethylmagnesium bromide was added to the solution at 0° C., and the mixture was stirred at 0° C. for one hr. Water (1 ml) was added dropwise to the reaction solution to stop the reaction. The mixture was extracted with ethyl acetate, and the ethyl acetate layer was then washed with water and saturated brine and was dried over anhydrous sodium sulfate. The solvent was removed by distillation under the reduced pressure to give 1-{2-[(6,7-dimethoxy-4-quinolyl)oxy]-5-iodophenyl}-1-propanol.

来源与证据

DOI10.6084/m9.figshare.5104873.v1
专利号US07560558B2
来源数据集uspto-grants-2009_07
ORD IDord-4ad7f767f5a347988f581a69730af127
来源说明uspto-grants-2009_07