反应详情

温度

60 °C

A 1 N sodium hydroxide aqueous solution (0.071 mL, 0.071 mmol) was added to a solution of (4′-{1-ethyl-1-[3-methyl-4-((E)-4,4,4-trifluoro-3-hydroxy-3-trifluoromethyl-1-butenyl)-phenyl]-propyl}-2′-methyl-biphenyl-4-yl)acetic acid methyl ester (Example 46-(1); 14.1 mg, 0.024 mmol) in methanol-tetrahydrofuran (1:1, 1 mL), and the mixture was stirred at 60° C. for one hour. Then, the reaction mixture was concentrated under reduced pressure. The resulting residue was purified by silica gel chromatography (chloroform:methanol=10:3, saturated with water) to give the target compound as a colorless oil (8.4 mg, 61%).

1. concentrationThen, the reaction mixture was concentrated under reduced pressure
2. customThe resulting residue was purified by silica gel chromatography (chloroform:methanol=10:3, saturated with water)