反应详情

温度

50 °C

p-Toluenesulfonic acid monohydrate (223 mg, 1.18 mmol) was added to a solution of allyl (4′-{[2-(dimethoxymethyl)-3-(methoxymethoxy)-4-(trifluoromethyl)benzyl]oxy}-3′-fluoro-1,1′-biphenyl-4-yl)acetate (618 mg, 1.06 mmol) obtained in Example (12-3) in acetone (10 ml), and the mixture was stirred at 50° C. for 1 hour. The residue obtained by concentrating the reaction mixture was diluted with ethyl acetate. The obtained solution was successively washed with a saturated aqueous sodium hydrogencarbonate solution, water and a saturated aqueous NaCl solution and dried with anhydrous sodium sulfate. The residue obtained by removing the solvent under reduced pressure was purified by silica gel column chromatography (eluting solvent: n-hexane/ethyl acetate=3/1) to give allyl (3′-fluoro-4′-{[2-formyl-3-hydroxy-4-(trifluoromethyl)benzyl]oxy}-1,1′-biphenyl-4-yl)acetate (476 mg, yield: 91%).

1. customThe residue obtained
2. concentrationby concentrating the reaction mixture
3. additionwas diluted with ethyl acetate
4. washThe obtained solution was successively washed with a saturated aqueous sodium hydrogencarbonate solution, water
5. dry with materiala saturated aqueous NaCl solution and dried with anhydrous sodium sulfate
6. customThe residue obtained
7. customby removing the solvent under reduced pressure
8. customwas purified by silica gel column chromatography (eluting solvent: n-hexane/ethyl acetate=3/1)