Реакция #1755494
ord-e4d0d7809cda4c369d984e307ee60e2c
Уравнение реакции
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Условия реакции
Обработка
- 1Экстракцияthe resulting mixture was extracted with ethyl acetate
- 2ПромывкаThe organic layer was washed with a saturated aqueous sodium hydrogen carbonate solution and brine
- 3Сушкаdried over anhydrous magnesium sulfate
- 4ДругоеThe solvent was removed under reduced pressure
- 5Другоеthe residue was purified by column chromatography on silica gel (eluent: hexane/ethyl acetate 1/1)
Методика
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).