反応 #1914831
ord-789f3f39b9914727ae4e22e2b70e7a52
反応方程式
4-[(4-methoxyphenyl)methyl]-5-methyl-3-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyloxy)-1H-pyrazole
potassium carbonate
iodomethane
→
4-[(4-methoxyphenyl)methyl]-1,5-dimethyl-3-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyloxy)pyrazole
収率 21.7%
反応物
試薬
なし
反応条件
温度
75°CELSIUS
詳細条件
See reaction.notes.procedure_details.
後処理
- 1ろ過The reaction mixture was filtered through celite®
- 2その他the solvent of the filtrate was removed under reduced pressure
- 3その他The residue was purified by preparative thin layer chromatography (developing solvent: benzene/acetone=2/1)
実験手順
A suspension of 4-[(4-methoxyphenyl)methyl]-5-methyl-3-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyloxy)-1H-pyrazole (18 mg), potassium carbonate (14 mg) and iodomethane (4.7 mg) in acetonitrile (2 mL) was stirred at 75° C. overnight. The reaction mixture was filtered through celite®, and the solvent of the filtrate was removed under reduced pressure. The residue was purified by preparative thin layer chromatography (developing solvent: benzene/acetone=2/1) to give 4-[(4-methoxyphenyl)methyl]-1,5-dimethyl-3-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyloxy)pyrazole (4 mg).