反応 #1755494
ord-e4d0d7809cda4c369d984e307ee60e2c
反応方程式
反応物
試薬
反応条件
後処理
- 1抽出the resulting mixture was extracted with ethyl acetate
- 2洗浄The organic layer was washed with a saturated aqueous sodium hydrogen carbonate solution and brine
- 3乾燥dried over anhydrous magnesium sulfate
- 4その他The solvent was removed under reduced pressure
- 5その他the residue was purified by column chromatography on silica gel (eluent: hexane/ethyl acetate 1/1)
実験手順
To a solution of 1,2-dihydro-4-[(4-methylthiophenyl)-methyl]-5-trifluoromethyl-3H-pyrazol-3-one (2.0 g) in acetonitrile (100 mL) were added acetobromo-α-D-glucose (3.1 g) and potassium carbonate (1.1 g), and the mixture was stirred at room temperature overnight. Water was added to the reaction mixture, and the resulting mixture was extracted with ethyl acetate. The organic layer was washed with a saturated aqueous sodium hydrogen carbonate solution and brine and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure, and the residue was purified by column chromatography on silica gel (eluent: hexane/ethyl acetate 1/1) to give 4-[(4-methylthiophenyl)methyl]-3-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyloxy)-5-trifluoromethyl-1H-pyrazole (2.0 g).